Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001275.3 | 664 | Missense Mutation | ACG,GCG | T18A | NP_001266.1 |
NM_001301690.1 | 664 | Missense Mutation | ACG,GCG | T18A | NP_001288619.1 |
XM_011536370.1 | 664 | Missense Mutation | ACG,GCG | T18A | XP_011534672.1 |