Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_024939.2 | 2088 | Missense Mutation | CAC,CGC | H667R | NP_079215.2 |
XM_005256153.4 | 2088 | Missense Mutation | CAC,CGC | H666R | XP_005256210.1 |
XM_006721273.3 | 2088 | Missense Mutation | CAC,CGC | H541R | XP_006721336.1 |
XM_011523338.2 | 2088 | Missense Mutation | CAC,CGC | H541R | XP_011521640.1 |