Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001012270.1 | 368 | Intron | NP_001012270.1 | ||
NM_001012271.1 | 368 | Missense Mutation | AGT,GGT | S106G | NP_001012271.1 |
NM_001168.2 | 368 | Missense Mutation | AGT,GGT | S83G | NP_001159.2 |