| 
                  NM_145038.5:c.1067C>T
                    
                              MANE Select
                      
               | 
              
                  
                    NP_659475.2:p.Ala356Val
                      
                  
               | 
            
            
              | 
                  ENST00000288710.7:c.1067C>T
                    
                        MANE Select
                      
               | 
              
                  
                    ENSP00000288710.2:p.Ala356Val
                      
                  
               | 
            
            
              | 
                  NM_145038.3:c.1067C>T
               | 
              
                  
                    NP_659475.2:p.Ala356Val
                      
                  
               | 
            
            
              | 
                  NM_145038.4:c.1067C>T
               | 
              
                  
                    NP_659475.2:p.Ala356Val
                      
                  
               | 
            
            
              | 
                  ENST00000288710.6:c.1067C>T
               | 
              
                  
                    ENSP00000288710.2:p.Ala356Val
                      
                  
               | 
            
            
              | 
                  ENST00000421869.5:c.*380C>T
               | 
              
                  
                    ENSP00000414375.1:n.*380C>T
                  
               | 
            
            
              | 
                  ENST00000483675.1:n.668C>T
               | 
              
                  
               | 
            
            
              | 
                  ENST00000649059.1:c.913C>T
               | 
              
                  
               | 
            
            
              | 
                  XM_005264637.3:c.449C>T
               | 
              
                  
                    XP_005264694.1:p.Ala150Val
                      
                  
               | 
            
            
              | 
                  XM_005264638.3:c.47C>T
               | 
              
                  
                    XP_005264695.1:p.Ala16Val
                      
                  
               | 
            
            
              | 
                  XM_017005271.1:c.47C>T
               | 
              
                  
                    XP_016860760.1:p.Ala16Val
                      
                  
               | 
            
            
              | 
                  XM_024453218.1:c.47C>T
               | 
              
                  
                    XP_024308986.1:p.Ala16Val
                      
                  
               |