| NM_000102.4:c.403T>G
                    
                              MANE Select | NP_000093.1:p.Phe135Val | 
            
              | ENST00000369887.4:c.403T>G
                    
                        MANE Select | ENSP00000358903.3:p.Phe135Val | 
            
              | NM_000102.3:c.403T>G | NP_000093.1:p.Phe135Val | 
            
              | ENST00000369887.3:c.403T>G | ENSP00000358903.3:p.Phe135Val | 
            
              | ENST00000489268.1:n.657T>G |  | 
            
              | ENST00000638190.1:c.403T>G | ENSP00000492539.1:p.Phe135Val | 
            
              | ENST00000638272.1:c.297+1778T>G | ENSP00000491508.1:n.297+1778T>G | 
            
              | ENST00000638971.1:c.403T>G | ENSP00000492313.1:p.Phe135Val | 
            
              | ENST00000639393.1:c.403T>G | ENSP00000492651.1:p.Phe135Val | 
            
              | ENST00000640633.1:n.165T>G |  |