Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_015117.2 | 2656 | Missense Mutation | TCC,TTC | S876F | NP_055932.2 |
XM_006716536.3 | 2656 | Missense Mutation | TCC,TTC | S938F | XP_006716599.2 |
XM_011516943.2 | 2656 | Intron | XP_011515245.1 | ||
XM_011516944.2 | 2656 | Intron | XP_011515246.1 | ||
XM_017013248.1 | 2656 | Missense Mutation | TCC,TTC | S1004F | XP_016868737.1 |
XM_017013249.1 | 2656 | Missense Mutation | TCC,TTC | S1004F | XP_016868738.1 |