| NM_000306.4:c.428G=
                    
                              MANE Select | NP_000297.1:p.Arg143= | 
            
              | ENST00000350375.7:c.428G=
                    
                        MANE Select | ENSP00000263781.2:p.Arg143= | 
            
              | NM_000306.3:c.428G= | NP_000297.1:p.Arg143= | 
            
              | NM_001122757.2:c.506G= | NP_001116229.1:p.Arg169= | 
            
              | NM_001122757.3:c.506G= | NP_001116229.1:p.Arg169= | 
            
              | ENST00000344265.7:c.506G= | ENSP00000342931.3:p.Arg169= | 
            
              | ENST00000344265.8:c.506G= | ENSP00000342931.3:p.Arg169= | 
            
              | ENST00000350375.6:c.428G= | ENSP00000263781.2:p.Arg143= | 
            
              | ENST00000560656.1:c.428G= | ENSP00000452610.1:p.Arg143= | 
            
              | ENST00000561167.5:c.215-2064G= | ENSP00000454072.1:n.215-2064G= |