Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001297701.1 | 502 | Missense Mutation | CCG,CGG | P122R | NP_001284630.1 |
NM_032878.3 | 502 | Missense Mutation | CCG,CGG | P150R | NP_116267.3 |
NM_198867.1 | 502 | Intron | NP_942567.1 | ||
XM_005259357.4 | 502 | Missense Mutation | CCG,CGG | P122R | XP_005259414.1 |