Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_015897.3 | 462 | Missense Mutation | CAG,CCG | Q100P | NP_056981.2 |
XM_011528060.2 | 462 | Missense Mutation | CAG,CCG | Q119P | XP_011526362.1 |
XM_017026868.1 | 462 | UTR 5 | XP_016882357.1 |