Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_174937.3 | 1732 | Missense Mutation | CAG,CGG | Q549R | NP_777597.2 |
XM_011539577.1 | 1732 | Missense Mutation | CAG,CGG | Q562R | XP_011537879.1 |
XM_011539578.2 | 1732 | Intron | XP_011537880.1 |