Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001287584.1 | 278 | Intron | NP_001274513.1 | ||
NM_001287585.1 | 278 | Intron | NP_001274514.1 | ||
NM_138285.4 | 278 | Intron | NP_612142.2 | ||
XM_006712254.2 | 278 | Intron | XP_006712317.1 | ||
XM_011510576.2 | 278 | Intron | XP_011508878.1 | ||
XM_011510577.2 | 278 | Intron | XP_011508879.1 | ||
XM_017003308.1 | 278 | Missense Mutation | CCG,TCG | P10S | XP_016858797.1 |