Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001317062.1 | 852 | Missense Mutation | TCC,TTC | S238F | NP_001303991.1 |
NM_001317063.1 | 852 | Missense Mutation | TCC,TTC | S238F | NP_001303992.1 |
NM_001317064.1 | 852 | Missense Mutation | TCC,TTC | S174F | NP_001303993.1 |
NM_024102.3 | 852 | Missense Mutation | TCC,TTC | S238F | NP_077007.1 |