| 
                  NM_015910.7:c.1237A>G
                    
                              MANE Select
                      
               | 
              
                  
                    NP_056994.3:p.Ile413Val
                      
                  
               | 
            
            
              | 
                  ENST00000272321.12:c.1237A>G
                    
                        MANE Select
                      
               | 
              
                  
                    ENSP00000272321.7:p.Ile413Val
                      
                  
               | 
            
            
              | 
                  NM_001042692.2:c.760A>G
               | 
              
                  
                    NP_001036157.1:p.Ile254Val
                      
                  
               | 
            
            
              | 
                  NM_001042692.3:c.760A>G
               | 
              
                  
                    NP_001036157.1:p.Ile254Val
                      
                  
               | 
            
            
              | 
                  NM_001354044.1:c.1165A>G
               | 
              
                  
                    NP_001340973.1:p.Ile389Val
                      
                  
               | 
            
            
              | 
                  NM_001354044.2:c.1165A>G
               | 
              
                  
                    NP_001340973.1:p.Ile389Val
                      
                  
               | 
            
            
              | 
                  NM_001354045.1:c.1237A>G
               | 
              
                  
                    NP_001340974.1:p.Ile413Val
                      
                  
               | 
            
            
              | 
                  NM_001354045.2:c.1237A>G
               | 
              
                  
                    NP_001340974.1:p.Ile413Val
                      
                  
               | 
            
            
              | 
                  NM_015910.5:c.1237A>G
               | 
              
                  
                    NP_056994.3:p.Ile413Val
                      
                  
               | 
            
            
              | 
                  NM_015910.6:c.1237A>G
               | 
              
                  
                    NP_056994.3:p.Ile413Val
                      
                  
               | 
            
            
              | 
                  NR_122106.1:n.884A>G
               | 
              
                  
               | 
            
            
              | 
                  NR_122106.2:n.884A>G
               | 
              
                  
               | 
            
            
              | 
                  NR_148704.1:n.2017A>G
               | 
              
                  
               | 
            
            
              | 
                  NR_148704.2:n.1695A>G
               | 
              
                  
               | 
            
            
              | 
                  NR_148705.1:n.1765A>G
               | 
              
                  
               | 
            
            
              | 
                  NR_148705.2:n.1443A>G
               | 
              
                  
               | 
            
            
              | 
                  ENST00000272321.11:c.1237A>G
               | 
              
                  
                    ENSP00000272321.7:p.Ile413Val
                      
                  
               | 
            
            
              | 
                  ENST00000398544.7:c.760A>G
               | 
              
                  
                    ENSP00000381552.3:p.Ile254Val
                      
                  
               | 
            
            
              | 
                  ENST00000409120.5:c.661A>G
               | 
              
                  
                    ENSP00000386769.1:p.Ile221Val
                      
                  
               | 
            
            
              | 
                  ENST00000409199.5:c.661A>G
               | 
              
                  
                    ENSP00000386592.1:p.Ile221Val
                      
                  
               | 
            
            
              | 
                  ENST00000409354.6:c.598A>G
               | 
              
                  
                    ENSP00000386795.2:p.Ile200Val
                      
                  
               | 
            
            
              | 
                  ENST00000409562.7:c.1237A>G
               | 
              
                  
                    ENSP00000387222.3:p.Ile413Val
                      
                  
               | 
            
            
              | 
                  ENST00000409835.5:n.1484A>G
               | 
              
                  
               | 
            
            
              | 
                  ENST00000417238.5:c.*1348A>G
               | 
              
                  
                    ENSP00000411429.1:n.*1348A>G
                  
               | 
            
            
              | 
                  ENST00000493315.1:n.939A>G
               | 
              
                  
               | 
            
            
              | 
                  XM_005264348.2:c.1237A>G
               | 
              
                  
                    XP_005264405.1:p.Ile413Val
                      
                  
               | 
            
            
              | 
                  XM_005264348.4:c.1237A>G
               | 
              
                  
                    XP_005264405.1:p.Ile413Val
                      
                  
               | 
            
            
              | 
                  XM_011532881.1:c.1165A>G
               | 
              
                  
                    XP_011531183.1:p.Ile389Val
                      
                  
               | 
            
            
              | 
                  XM_011532881.3:c.1165A>G
               | 
              
                  
                    XP_011531183.1:p.Ile389Val
                      
                  
               | 
            
            
              | 
                  XM_011532882.1:c.1138A>G
               | 
              
                  
                    XP_011531184.1:p.Ile380Val
                      
                  
               | 
            
            
              | 
                  XM_011532883.1:c.1237A>G
               | 
              
                  
                    XP_011531185.1:p.Ile413Val
                      
                  
               | 
            
            
              | 
                  XM_011532884.1:c.1237A>G
               | 
              
                  
                    XP_011531186.1:p.Ile413Val
                      
                  
               | 
            
            
              | 
                  XM_011532884.3:c.1237A>G
               | 
              
                  
                    XP_011531186.1:p.Ile413Val
                      
                  
               | 
            
            
              | 
                  XM_011532885.1:c.1237A>G
               | 
              
                  
                    XP_011531187.1:p.Ile413Val
                      
                  
               | 
            
            
              | 
                  XM_011532886.1:c.1237A>G
               | 
              
                  
                    XP_011531188.1:p.Ile413Val
                      
                  
               | 
            
            
              | 
                  XM_011532887.1:c.1237A>G
               | 
              
                  
                    XP_011531189.1:p.Ile413Val
                      
                  
               | 
            
            
              | 
                  XM_011532887.3:c.1237A>G
               | 
              
                  
                    XP_011531189.1:p.Ile413Val
                      
                  
               | 
            
            
              | 
                  XM_011532888.1:c.1237A>G
               | 
              
                  
                    XP_011531190.1:p.Ile413Val
                      
                  
               | 
            
            
              | 
                  XM_011532889.1:c.1237A>G
               | 
              
                  
                    XP_011531191.1:p.Ile413Val
                      
                  
               | 
            
            
              | 
                  XM_011532890.1:c.1237A>G
               | 
              
                  
                    XP_011531192.1:p.Ile413Val
                      
                  
               | 
            
            
              | 
                  XM_011532890.3:c.1237A>G
               | 
              
                  
                    XP_011531192.1:p.Ile413Val
                      
                  
               | 
            
            
              | 
                  XM_011532891.1:c.1165A>G
               | 
              
                  
                    XP_011531193.1:p.Ile389Val
                      
                  
               | 
            
            
              | 
                  XM_011532891.2:c.1165A>G
               | 
              
                  
                    XP_011531193.1:p.Ile389Val
                      
                  
               | 
            
            
              | 
                  XM_017004253.2:c.1237A>G
               | 
              
                  
                    XP_016859742.1:p.Ile413Val
                      
                  
               | 
            
            
              | 
                  XM_017004254.2:c.1237A>G
               | 
              
                  
                    XP_016859743.1:p.Ile413Val
                      
                  
               | 
            
            
              | 
                  XR_001738759.2:n.1699A>G
               | 
              
                  
               | 
            
            
              | 
                  XR_001738760.2:n.1699A>G
               | 
              
                  
               | 
            
            
              | 
                  XR_002959303.1:n.1699A>G
               | 
              
                  
               | 
            
            
              | 
                  XR_244934.1:n.1484A>G
               | 
              
                  
               | 
            
            
              | 
                  XR_244934.3:n.1699A>G
               | 
              
                  
               | 
            
            
              | 
                  XR_244935.1:n.1484A>G
               | 
              
                  
               | 
            
            
              | 
                  XR_939686.1:n.1484A>G
               | 
              
                  
               |