Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_080660.3 | 1132 | Missense Mutation | CCG,TCG | P259S | NP_542391.2 |
XM_006716176.3 | 1132 | UTR 3 | XP_006716239.1 | ||
XM_011516688.2 | 1132 | Missense Mutation | CCG,TCG | P259S | XP_011514990.1 |
XM_011516689.2 | 1132 | Missense Mutation | CCG,TCG | P123S | XP_011514991.1 |