Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001100592.2 | 988 | Missense Mutation | AGT,GGT | S13G | NP_001094062.1 |
NM_001289990.1 | 988 | Missense Mutation | AGT,GGT | S13G | NP_001276919.1 |
NM_145230.3 | 988 | Missense Mutation | AGT,GGT | S13G | NP_660265.2 |