Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_018994.2 | 2170 | Missense Mutation | ACG,ATG | T639M | NP_061867.1 |
XM_006710698.3 | 2170 | Missense Mutation | ACG,ATG | T639M | XP_006710761.1 |
XM_017001502.1 | 2170 | Missense Mutation | ACG,ATG | T408M | XP_016856991.1 |
XM_017001503.1 | 2170 | Missense Mutation | ACG,ATG | T408M | XP_016856992.1 |