| 
                  NM_005921.2:c.1846G>C
                    
                              MANE Select
                      
               | 
              
                  
                    NP_005912.1:p.Gly616Arg
                      
                  
               | 
            
            
              | 
                  ENST00000399503.4:c.1846G>C
                    
                        MANE Select
                      
               | 
              
                  
                    ENSP00000382423.3:p.Gly616Arg
                      
                  
               | 
            
            
              | 
                  NM_005921.1:c.1846G>C
               | 
              
                  
                    NP_005912.1:p.Gly616Arg
                      
                  
               | 
            
            
              | 
                  ENST00000399503.3:c.1846G>C
               | 
              
                  
                    ENSP00000382423.3:p.Gly616Arg
                      
                  
               | 
            
            
              | 
                  XM_005248519.3:c.1468G>C
               | 
              
                  
                    XP_005248576.2:p.Gly490Arg
                      
                  
               | 
            
            
              | 
                  XM_011543406.1:c.1591G>C
               | 
              
                  
                    XP_011541708.1:p.Gly531Arg
                      
                  
               | 
            
            
              | 
                  XM_011543407.1:c.1686+2186G>C
               | 
              
                  
                    XP_011541709.1:n.1686+2186G>C
                  
               | 
            
            
              | 
                  XM_011543408.1:c.1846G>C
               | 
              
                  
                    XP_011541710.1:p.Gly616Arg
                      
                  
               | 
            
            
              | 
                  XM_017009484.1:c.1435G>C
               | 
              
                  
                    XP_016864973.1:p.Gly479Arg
                      
                  
               | 
            
            
              | 
                  XM_017009485.1:c.1357G>C
               | 
              
                  
                    XP_016864974.1:p.Gly453Arg
                      
                  
               | 
            
            
              | 
                  XR_001742068.2:n.1877G>C
               | 
              
                  
               |