Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001009992.1 | 5577 | Missense Mutation | ACG,ATG | T479M | NP_001009992.1 |
XM_017000301.1 | 5577 | Missense Mutation | ACG,ATG | T479M | XP_016855790.1 |
XM_017000302.1 | 5577 | Missense Mutation | ACG,ATG | T479M | XP_016855791.1 |