| 
                  NM_000088.4:c.934C>T
                    
                              MANE Select
                      
               | 
              
                  
                    NP_000079.2:p.Arg312Cys
                      
                  
               | 
            
            
              | 
                  ENST00000225964.10:c.934C>T
                    
                        MANE Select
                      
               | 
              
                  
                    ENSP00000225964.6:p.Arg312Cys
                      
                  
               | 
            
            
              | 
                  NM_000088.3:c.934C>T , LRG_1t1:c.934C>T
               | 
              
                  
                    NP_000079.2:p.Arg312Cys
                      
                  
               | 
            
            
              | 
                  ENST00000225964.9:c.934C>T
               | 
              
                  
                    ENSP00000225964.5:p.Arg312Cys
                      
                  
               | 
            
            
              | 
                  ENST00000485870.1:n.259C>T
               | 
              
                  
               | 
            
            
              | 
                  XM_005257058.3:c.934C>T
               | 
              
                  
                    XP_005257115.2:p.Arg312Cys
                      
                  
               | 
            
            
              | 
                  XM_005257058.4:c.934C>T
               | 
              
                  
                    XP_005257115.2:p.Arg312Cys
                      
                  
               | 
            
            
              | 
                  XM_005257059.3:c.934C>T
               | 
              
                  
                    XP_005257116.2:p.Arg312Cys
                      
                  
               | 
            
            
              | 
                  XM_005257059.4:c.934C>T
               | 
              
                  
                    XP_005257116.2:p.Arg312Cys
                      
                  
               | 
            
            
              | 
                  XM_011524341.1:c.934C>T
               | 
              
                  
                    XP_011522643.1:p.Arg312Cys
                      
                  
               |