Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001271680.1 | 554 | Intron | NP_001258609.1 | ||
NM_021118.2 | 554 | Missense Mutation | CAT,CGT | H167R | NP_066941.1 |
XM_005262086.3 | 554 | Missense Mutation | CAT,CGT | H166R | XP_005262143.1 |