Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000481.3 | 752 | Missense Mutation | CAC,CGC | H219R | NP_000472.2 |
NM_001164710.1 | 752 | Missense Mutation | CAC,CGC | H175R | NP_001158182.1 |
NM_001164711.1 | 752 | Missense Mutation | CAC,CGC | H163R | NP_001158183.1 |
NM_001164712.1 | 752 | Missense Mutation | CAC,CGC | H219R | NP_001158184.1 |