Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000215.3 | 3466 | Silent Mutation | TCC,TCT | S1122S | NP_000206.2 |
XM_005259896.3 | 3466 | Silent Mutation | TCC,TCT | S1165S | XP_005259953.1 |
XM_011527990.1 | 3466 | Intron | XP_011526292.1 | ||
XM_011527991.2 | 3466 | Intron | XP_011526293.1 |