Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_033452.2 | 1418 | Missense Mutation | CAC,CGC | H464R | NP_258411.2 |
XM_005257787.4 | 1418 | Missense Mutation | CAC,CGC | H226R | XP_005257844.1 |
XM_005257788.4 | 1418 | Missense Mutation | CAC,CGC | H226R | XP_005257845.1 |