| NM_000101.4:c.281A>G
                    
                              MANE Select | NP_000092.2:p.His94Arg | 
            
              | ENST00000261623.8:c.281A>G
                    
                        MANE Select | ENSP00000261623.3:p.His94Arg | 
            
              | NM_000101.3:c.281A>G | NP_000092.2:p.His94Arg | 
            
              | ENST00000261623.7:c.281A>G | ENSP00000261623.3:p.His94Arg | 
            
              | ENST00000562209.1:n.561A>G |  | 
            
              | ENST00000563526.5:n.256A>G |  | 
            
              | ENST00000565588.5:c.65A>G |  | 
            
              | ENST00000565588.6:c.281A>G | ENSP00000455537.2:p.His94Arg | 
            
              | ENST00000566229.1:c.270A>G | ENSP00000457060.1:p.Ala90= | 
            
              | ENST00000566534.5:n.303A>G |  | 
            
              | ENST00000567174.5:c.281A>G | ENSP00000454951.1:p.His94Arg | 
            
              | ENST00000568278.1:c.281A>G | ENSP00000455506.1:p.His94Arg | 
            
              | ENST00000569359.5:c.281A>G | ENSP00000456079.1:p.His94Arg | 
            
              | ENST00000696156.1:c.203+340A>G | ENSP00000512446.1:n.203+340A>G | 
            
              | ENST00000696157.1:c.281A>G | ENSP00000512447.1:p.His94Arg | 
            
              | ENST00000696158.1:c.281A>G | ENSP00000512448.1:p.His94Arg | 
            
              | ENST00000696159.1:c.281A>G | ENSP00000512449.1:p.His94Arg | 
            
              | ENST00000696160.1:c.281A>G | ENSP00000512450.1:p.His94Arg | 
            
              | ENST00000696161.1:c.411A>G | ENSP00000512451.1:p.Ala137= | 
            
              | ENST00000696162.1:c.281A>G | ENSP00000512452.1:p.His94Arg | 
            
              | ENST00000696163.1:c.230A>G | ENSP00000512453.1:p.His77Arg | 
            
              | XM_011522905.1:c.281A>G | XP_011521207.1:p.His94Arg | 
            
              | XM_011522905.3:c.281A>G | XP_011521207.1:p.His94Arg |