Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001127460.2 | 3438 | Missense Mutation | GGT,TGT | G1021C | NP_001120932.1 |
NM_001166279.1 | 3438 | Missense Mutation | GGT,TGT | G1020C | NP_001159751.1 |
NM_014871.4 | 3438 | Missense Mutation | GGT,TGT | G1017C | NP_055686.3 |