Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_019849.2 | 1659 | Missense Mutation | CAC,CGC | H410R | NP_062823.1 |
XM_006723284.2 | 1659 | Intron | XP_006723347.1 | ||
XM_011527119.1 | 1659 | Missense Mutation | CAC,CGC | H547R | XP_011525421.1 |
XM_011527120.1 | 1659 | Missense Mutation | CAC,CGC | H520R | XP_011525422.1 |