Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001321770.1 | 668 | Missense Mutation | ACG,CCG | T81P | NP_001308699.1 |
NM_006588.3 | 668 | Missense Mutation | ACG,CCG | T81P | NP_006579.2 |
XM_017003807.1 | 668 | UTR 5 | XP_016859296.1 |