| NM_005202.4:c.1328C>T
                    
                              MANE Select | NP_005193.1:p.Ala443Val | 
            
              | ENST00000397799.2:c.1328C>T
                    
                        MANE Select | ENSP00000380901.1:p.Ala443Val | 
            
              | NM_001294347.1:c.1133C>T | NP_001281276.1:p.Ala378Val | 
            
              | NM_001294347.2:c.1133C>T | NP_001281276.1:p.Ala378Val | 
            
              | NM_005202.3:c.1328C>T | NP_005193.1:p.Ala443Val | 
            
              | ENST00000303143.9:c.1328C>T | ENSP00000305913.4:p.Ala443Val | 
            
              | ENST00000397799.1:c.1328C>T | ENSP00000380901.1:p.Ala443Val | 
            
              | ENST00000481785.1:c.1133C>T | ENSP00000436433.1:p.Ala378Val | 
            
              | ENST00000615990.1:c.773-273C>T | ENSP00000484406.1:n.773-273C>T | 
            
              | XM_005270477.2:c.1559C>T | XP_005270534.1:p.Ala520Val | 
            
              | XM_005270477.3:c.1559C>T | XP_005270534.1:p.Ala520Val |