| NM_004415.4:c.2821C>T
                    
                              MANE Select | NP_004406.2:p.Arg941Ter | 
            
              | ENST00000379802.8:c.2821C>T
                    
                        MANE Select | ENSP00000369129.3:p.Arg941Ter | 
            
              | NM_001008844.1:c.2821C>T | NP_001008844.1:p.Arg941Ter | 
            
              | NM_001008844.2:c.2821C>T | NP_001008844.1:p.Arg941Ter | 
            
              | NM_001008844.3:c.2821C>T | NP_001008844.1:p.Arg941Ter | 
            
              | NM_001319034.1:c.2821C>T | NP_001305963.1:p.Arg941Ter | 
            
              | NM_001319034.2:c.2821C>T | NP_001305963.1:p.Arg941Ter | 
            
              | NM_004415.2:c.2821C>T , LRG_423t1:c.2821C>T | NP_004406.2:p.Arg941Ter | 
            
              | NM_004415.3:c.2821C>T | NP_004406.2:p.Arg941Ter | 
            
              | ENST00000379802.7:c.2821C>T | ENSP00000369129.3:p.Arg941Ter | 
            
              | ENST00000418664.2:c.2821C>T | ENSP00000396591.2:p.Arg941Ter | 
            
              | ENST00000710359.1:c.2821C>T | ENSP00000518230.1:p.Arg941Ter | 
            
              | XM_011514323.1:c.2821C>T | XP_011512625.1:p.Arg941Ter |