| 
                  NM_006218.4:c.2592C>T
                    
                              MANE Select
                      
               | 
              
                  
                    NP_006209.2:p.Gly864=
                  
               | 
            
            
              | 
                  ENST00000263967.4:c.2592C>T
                    
                        MANE Select
                      
               | 
              
                  
                    ENSP00000263967.3:p.Gly864=
                  
               | 
            
            
              | 
                  NM_006218.2:c.2592C>T , LRG_310t1:c.2592C>T
               | 
              
                  
                    NP_006209.2:p.Gly864=
                  
               | 
            
            
              | 
                  NM_006218.3:c.2592C>T
               | 
              
                  
                    NP_006209.2:p.Gly864=
                  
               | 
            
            
              | 
                  ENST00000263967.3:c.2592C>T
               | 
              
                  
                    ENSP00000263967.3:p.Gly864=
                  
               | 
            
            
              | 
                  ENST00000462255.2:n.1054C>T
               | 
              
                  
               | 
            
            
              | 
                  ENST00000643187.1:c.2592C>T
               | 
              
                  
                    ENSP00000493507.1:p.Gly864=
                  
               | 
            
            
              | 
                  ENST00000674534.1:n.3500C>T
               | 
              
                  
               | 
            
            
              | 
                  ENST00000674622.1:c.1013C>T
               | 
              
                  
                    ENSP00000502417.1:n.1013C>T
                  
               | 
            
            
              | 
                  ENST00000675467.1:n.5399C>T
               | 
              
                  
               | 
            
            
              | 
                  ENST00000675786.1:c.*1159C>T
               | 
              
                  
                    ENSP00000502323.1:n.*1159C>T
                  
               | 
            
            
              | 
                  ENST00000675796.1:n.2487C>T
               | 
              
                  
               | 
            
            
              | 
                  XM_006713658.2:c.2592C>T
               | 
              
                  
                    XP_006713721.1:p.Gly864=
                  
               | 
            
            
              | 
                  XM_006713658.4:c.2592C>T
               | 
              
                  
                    XP_006713721.1:p.Gly864=
                  
               | 
            
            
              | 
                  XM_011512894.1:c.2592C>T
               | 
              
                  
                    XP_011511196.1:p.Gly864=
                  
               | 
            
            
              | 
                  XM_011512894.2:c.2592C>T
               | 
              
                  
                    XP_011511196.1:p.Gly864=
                  
               |