Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001096.2 | 3163 | Missense Mutation | TCC,TTC | S998F | NP_001087.2 |
NM_001303274.1 | 3163 | Missense Mutation | TCC,TTC | S1052F | NP_001290203.1 |
NM_001303275.1 | 3163 | Missense Mutation | TCC,TTC | S1042F | NP_001290204.1 |
NM_198830.1 | 3163 | Missense Mutation | TCC,TTC | S988F | NP_942127.1 |
XM_005257395.1 | 3163 | Missense Mutation | TCC,TTC | S998F | XP_005257452.1 |
XM_017024688.1 | 3163 | Missense Mutation | TCC,TTC | S988F | XP_016880177.1 |