Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001317721.1 | 682 | Missense Mutation | ATG,CTG | M4L | NP_001304650.1 |
NM_152892.2 | 682 | Missense Mutation | ATG,CTG | M156L | NP_690852.1 |
XM_017011845.1 | 682 | UTR 5 | XP_016867334.1 |