Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_004308.3 | 1059 | Missense Mutation | CAC,CGC | H381R | NP_004299.1 |
XM_011520095.1 | 1059 | Missense Mutation | CAC,CGC | H381R | XP_011518397.1 |
XM_017017720.1 | 1059 | Missense Mutation | CAC,CGC | H337R | XP_016873209.1 |