Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_024589.2 | 1092 | Missense Mutation | CAC,CGC | H238R | NP_078865.1 |
XM_006720947.3 | 1092 | Missense Mutation | CAC,CGC | H245R | XP_006721010.1 |
XM_006720948.3 | 1092 | Missense Mutation | CAC,CGC | H155R | XP_006721011.1 |