Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001122961.1 | 663 | Missense Mutation | CAG,CGG | Q46R | NP_001116433.1 |
XM_005270448.3 | 663 | Intron | XP_005270505.1 | ||
XM_006710342.3 | 663 | Missense Mutation | CAG,CGG | Q157R | XP_006710405.1 |
XM_006710343.3 | 663 | Intron | XP_006710406.1 | ||
XM_011540647.2 | 663 | Missense Mutation | CAG,CGG | Q167R | XP_011538949.1 |
XM_011540648.1 | 663 | Missense Mutation | CAG,CGG | Q167R | XP_011538950.1 |