Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000951.2 | 229 | Missense Mutation | CCC,TCC | P22S | NP_000942.1 |
NM_001316335.1 | 229 | UTR 5 | NP_001303264.1 | ||
XM_006723286.2 | 229 | Missense Mutation | CCC,TCC | P22S | XP_006723349.1 |
XM_011527124.1 | 229 | UTR 5 | XP_011525426.1 |