Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_004638.3 | 621 | Missense Mutation | CAG,CCG | Q112P | NP_004629.3 |
NM_080686.2 | 621 | Missense Mutation | CAG,CCG | Q112P | NP_542417.2 |
XM_017011274.1 | 621 | Missense Mutation | CAG,CCG | Q112P | XP_016866763.1 |