Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_152377.2 | 1474 | Missense Mutation | CAG,CGG | Q519R | NP_689590.1 |
XM_017000307.1 | 1474 | Missense Mutation | CAG,CGG | Q471R | XP_016855796.1 |
XM_017000308.1 | 1474 | Intron | XP_016855797.1 |