Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_170607.2 | 166 | Missense Mutation | CAC,CGC | H88R | NP_733752.1 |
NM_198204.1 | 166 | Missense Mutation | CAC,CGC | H34R | NP_937847.1 |
NM_198205.1 | 166 | Intron | NP_937848.1 | ||
XM_017024991.1 | 166 | Intron | XP_016880480.1 |