Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_080866.2 | 662 | Missense Mutation | ATG,GTG | M132V | NP_543142.2 |
XM_017017159.1 | 662 | Missense Mutation | ATG,GTG | M132V | XP_016872648.1 |
XM_017017160.1 | 662 | UTR 5 | XP_016872649.1 |