| 
                  NM_000782.5:c.552C>T
                    
                              MANE Select
                      
               | 
              
                  
                    NP_000773.2:p.Ala184=
                  
               | 
            
            
              | 
                  ENST00000216862.8:c.552C>T
                    
                        MANE Select
                      
               | 
              
                  
                    ENSP00000216862.3:p.Ala184=
                  
               | 
            
            
              | 
                  NM_000782.4:c.552C>T
               | 
              
                  
                    NP_000773.2:p.Ala184=
                  
               | 
            
            
              | 
                  NM_001128915.1:c.552C>T
               | 
              
                  
                    NP_001122387.1:p.Ala184=
                  
               | 
            
            
              | 
                  NM_001128915.2:c.552C>T
               | 
              
                  
                    NP_001122387.1:p.Ala184=
                  
               | 
            
            
              | 
                  ENST00000216862.7:c.552C>T
               | 
              
                  
                    ENSP00000216862.3:p.Ala184=
                  
               | 
            
            
              | 
                  ENST00000395954.3:c.126C>T
               | 
              
                  
                    ENSP00000379284.3:p.Ala42=
                  
               | 
            
            
              | 
                  ENST00000395955.7:c.552C>T
               | 
              
                  
                    ENSP00000379285.3:p.Ala184=
                  
               | 
            
            
              | 
                  XM_005260304.3:c.552C>T
               | 
              
                  
                    XP_005260361.1:p.Ala184=
                  
               | 
            
            
              | 
                  XM_005260304.5:c.552C>T
               | 
              
                  
                    XP_005260361.1:p.Ala184=
                  
               | 
            
            
              | 
                  XM_017027691.2:c.552C>T
               | 
              
                  
                    XP_016883180.1:p.Ala184=
                  
               | 
            
            
              | 
                  XM_017027692.2:c.552C>T
               | 
              
                  
                    XP_016883181.1:p.Ala184=
                  
               | 
            
            
              | 
                  XM_017027693.2:c.552C>T
               | 
              
                  
                    XP_016883182.1:p.Ala184=
                  
               |