Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001318810.1 | 3032 | Missense Mutation | CAT,CGT | H863R | NP_001305739.1 |
NM_001318811.1 | 3032 | Missense Mutation | CAT,CGT | H863R | NP_001305740.1 |
NM_014926.3 | 3032 | Missense Mutation | CAT,CGT | H863R | NP_055741.2 |