Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000077.4 | 772 | Missense Mutation | ACG,GCG | T148A | NP_000068.1 |
NM_001195132.1 | 772 | Missense Mutation | ACG,GCG | T148A | NP_001182061.1 |
NM_058195.3 | 772 | UTR 3 | NP_478102.2 | ||
NM_058197.4 | 772 | UTR 3 | NP_478104.2 | ||
XM_005251343.1 | 772 | Missense Mutation | ACG,GCG | T97A | XP_005251400.1 |
XM_011517675.2 | 772 | Missense Mutation | ACG,GCG | T148A | XP_011515977.1 |
XM_011517676.2 | 772 | Missense Mutation | ACG,GCG | T148A | XP_011515978.1 |
XM_011517679.1 | 772 | Missense Mutation | ACG,GCG | T97A | XP_011515981.1 |