Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001009566.2 | 3450 | Missense Mutation | CAT,CGT | H886R | NP_001009566.1 |
NM_001302883.1 | 3450 | Missense Mutation | CAT,CGT | H867R | NP_001289812.1 |
NM_014944.4 | 3450 | Missense Mutation | CAT,CGT | H876R | NP_055759.3 |