Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001171968.1 | 2212 | Missense Mutation | GGC,GTC | G821V | NP_001165439.1 |
NM_021924.4 | 2212 | Missense Mutation | GGC,GTC | G827V | NP_068743.2 |
NM_031264.3 | 2212 | Missense Mutation | GGC,GTC | G633V | NP_112554.2 |
XM_006718253.3 | 2212 | Missense Mutation | GGC,GTC | G747V | XP_006718316.1 |
XM_011520188.2 | 2212 | Missense Mutation | GGC,GTC | G716V | XP_011518490.1 |
XM_011520189.2 | 2212 | Missense Mutation | GGC,GTC | G685V | XP_011518491.1 |
XM_011520190.2 | 2212 | UTR 3 | XP_011518492.1 | ||
XM_011520191.2 | 2212 | Intron | XP_011518493.1 |