| 
                  NM_000301.5:c.1366G>C
                    
                              MANE Select
                      
               | 
              
                  
                    NP_000292.1:p.Gly456Arg
                      
                  
               | 
            
            
              | 
                  ENST00000308192.14:c.1366G>C
                    
                        MANE Select
                      
               | 
              
                  
                    ENSP00000308938.9:p.Gly456Arg
                      
                  
               | 
            
            
              | 
                  NM_000301.3:c.1366G>C , LRG_571t1:c.1366G>C
               | 
              
                  
                    NP_000292.1:p.Gly456Arg
                      
                  
               | 
            
            
              | 
                  NM_000301.4:c.1366G>C
               | 
              
                  
                    NP_000292.1:p.Gly456Arg
                      
                  
               | 
            
            
              | 
                  ENST00000297289.8:n.364G>C
               | 
              
                  
               | 
            
            
              | 
                  ENST00000297289.9:c.319G>C
               | 
              
                  
                    ENSP00000516619.1:p.Gly107Arg
                      
                  
               | 
            
            
              | 
                  ENST00000308192.13:c.1366G>C
               | 
              
                  
                    ENSP00000308938.9:p.Gly456Arg
                      
                  
               | 
            
            
              | 
                  ENST00000418964.2:c.1417G>C
               | 
              
                  
                    ENSP00000389424.2:p.Gly473Arg
                      
                  
               | 
            
            
              | 
                  ENST00000493435.1:n.421G>C
               | 
              
                  
               | 
            
            
              | 
                  ENST00000706906.1:c.1366G>C
               | 
              
                  
                    ENSP00000516618.1:p.Gly456Arg
                      
                  
               |