Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001085447.1 | 1229 | Missense Mutation | GCT,GGT | A405G | NP_001078916.1 |
XM_011510589.1 | 1229 | Missense Mutation | GCT,GGT | A381G | XP_011508891.1 |
XM_011510590.1 | 1229 | Missense Mutation | GCT,GGT | A324G | XP_011508892.1 |