Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_174911.4 | 1082 | Missense Mutation | GCG,TCG | A185S | NP_777571.1 |
XM_017013107.1 | 1082 | Missense Mutation | GCG,TCG | A185S | XP_016868596.1 |
XM_017013108.1 | 1082 | Missense Mutation | GCG,TCG | A167S | XP_016868597.1 |