Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001161683.1 | 406 | Intron | NP_001155155.1 | ||
NM_144672.3 | 406 | Missense Mutation | TCC,TTC | S9F | NP_653273.3 |
NM_170664.2 | 406 | Intron | NP_733764.1 | ||
XM_011545747.2 | 406 | Missense Mutation | TCC,TTC | S9F | XP_011544049.1 |
XM_011545748.2 | 406 | Intron | XP_011544050.2 | ||
XM_017022950.1 | 406 | Missense Mutation | TCC,TTC | S9F | XP_016878439.1 |
XM_017022951.1 | 406 | Intron | XP_016878440.1 |