Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_007260.2 | 1063 | Intron | NP_009191.1 | ||
XM_005245728.4 | 1063 | Missense Mutation | CAG,CGG | Q204R | XP_005245785.1 |
XM_017000165.1 | 1063 | Missense Mutation | CAG,CGG | Q192R | XP_016855654.1 |