Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001271168.1 | 1333 | Missense Mutation | TCC,TTC | S296F | NP_001258097.1 |
NM_022760.4 | 1333 | Missense Mutation | TCC,TTC | S347F | NP_073597.2 |
XM_005260804.2 | 1333 | Missense Mutation | TCC,TTC | S347F | XP_005260861.1 |
XM_005260805.2 | 1333 | Missense Mutation | TCC,TTC | S296F | XP_005260862.1 |
XM_005260806.3 | 1333 | Intron | XP_005260863.1 |