Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_002235.3 | 1018 | Missense Mutation | CAC,CGC | H51R | NP_002226.1 |
XM_005253686.3 | 1018 | Missense Mutation | CAC,CGC | H51R | XP_005253743.1 |
XM_011520955.2 | 1018 | Missense Mutation | CAC,CGC | H51R | XP_011519257.1 |
XM_017019270.1 | 1018 | Missense Mutation | CAC,CGC | H51R | XP_016874759.1 |
XM_017019271.1 | 1018 | Missense Mutation | CAC,CGC | H51R | XP_016874760.1 |
XM_017019272.1 | 1018 | Missense Mutation | CAC,CGC | H51R | XP_016874761.1 |