| 
                  NM_000660.7:c.1159T>C
                    
                              MANE Select
                      
               | 
              
                  
                    NP_000651.3:p.Cys387Arg
                      
                  
               | 
            
            
              | 
                  ENST00000221930.6:c.1159T>C
                    
                        MANE Select
                      
               | 
              
                  
                    ENSP00000221930.4:p.Cys387Arg
                      
                  
               | 
            
            
              | 
                  NM_000660.5:c.1159T>C
               | 
              
                  
                    NP_000651.3:p.Cys387Arg
                      
                  
               | 
            
            
              | 
                  NM_000660.6:c.1159T>C
               | 
              
                  
                    NP_000651.3:p.Cys387Arg
                      
                  
               | 
            
            
              | 
                  ENST00000221930.5:c.1159T>C
               | 
              
                  
                    ENSP00000221930.4:p.Cys387Arg
                      
                  
               | 
            
            
              | 
                  ENST00000598758.5:c.302+1062T>C
               | 
              
                  
               | 
            
            
              | 
                  ENST00000600196.2:c.1099T>C
               | 
              
                  
                    ENSP00000504008.1:p.Cys367Arg
                      
                  
               | 
            
            
              | 
                  ENST00000677934.1:c.933T>C
               | 
              
                  
                    ENSP00000504769.1:n.933T>C
                  
               | 
            
            
              | 
                  XM_011527242.1:c.1162T>C
               | 
              
                  
                    XP_011525544.1:p.Cys388Arg
                      
                  
               | 
            
            
              | 
                  XM_011527242.2:c.1162T>C
               | 
              
                  
                    XP_011525544.1:p.Cys388Arg
                      
                  
               |