| NM_205768.3:c.1183C>T
                    
                              MANE Select | NP_991331.1:p.Gln395Ter | 
            
              | ENST00000358704.4:c.1183C>T
                    
                        MANE Select | ENSP00000351539.4:p.Gln395Ter | 
            
              | NM_001278196.1:c.1156C>T | NP_001265125.1:p.Gln386Ter | 
            
              | NM_001278196.2:c.1156C>T | NP_001265125.1:p.Gln386Ter | 
            
              | NM_006352.4:c.1156C>T | NP_006343.2:p.Gln386Ter | 
            
              | NM_205768.2:c.1183C>T | NP_991331.1:p.Gln395Ter | 
            
              | ENST00000622512.1:c.1156C>T | ENSP00000481278.1:p.Gln386Ter | 
            
              | ENST00000696615.1:c.*360C>T | ENSP00000512755.1:n.*360C>T | 
            
              | ENST00000696616.1:c.1156C>T | ENSP00000512756.1:p.Gln386Ter | 
            
              | ENST00000696617.1:c.*1113C>T | ENSP00000512757.1:n.*1113C>T | 
            
              | ENST00000696618.1:c.1156C>T | ENSP00000512758.1:p.Gln386Ter | 
            
              | XM_005273006.2:c.1156C>T | XP_005273063.1:p.Gln386Ter | 
            
              | XM_017000060.1:c.1156C>T | XP_016855549.1:p.Gln386Ter |