Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001303264.1 | 1842 | Missense Mutation | CCG,TCG | P276S | NP_001290193.1 |
NM_014779.3 | 1842 | Missense Mutation | CCG,TCG | P276S | NP_055594.1 |
XM_011513337.2 | 1842 | Missense Mutation | CCG,TCG | P276S | XP_011511639.1 |