Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001171653.1 | 3067 | Missense Mutation | TCC,TTC | S960F | NP_001165124.1 |
NM_014795.3 | 3067 | Missense Mutation | TCC,TTC | S984F | NP_055610.1 |
XM_006712881.3 | 3067 | Missense Mutation | TCC,TTC | S984F | XP_006712944.1 |
XM_006712882.3 | 3067 | Missense Mutation | TCC,TTC | S984F | XP_006712945.1 |
XM_011512232.2 | 3067 | Missense Mutation | TCC,TTC | S977F | XP_011510534.1 |
XM_017005414.1 | 3067 | Missense Mutation | TCC,TTC | S872F | XP_016860903.1 |
XM_017005415.1 | 3067 | Missense Mutation | TCC,TTC | S872F | XP_016860904.1 |