Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001015878.1 | 380 | Missense Mutation | CAT,CGT | H111R | NP_001015878.1 |
NM_001015879.1 | 380 | Missense Mutation | CAT,CGT | H92R | NP_001015879.1 |
NM_003160.2 | 380 | Missense Mutation | CAT,CGT | H77R | NP_003151.2 |