Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001145444.1 | 3028 | Missense Mutation | CCG,TCG | P868S | NP_001138916.1 |
NM_001145445.1 | 3028 | Missense Mutation | CCG,TCG | P861S | NP_001138917.1 |
NM_020706.2 | 3028 | Missense Mutation | CCG,TCG | P883S | NP_065757.1 |
XM_005261017.2 | 3028 | Missense Mutation | CCG,TCG | P824S | XP_005261074.1 |
XM_006724035.2 | 3028 | Missense Mutation | CCG,TCG | P879S | XP_006724098.1 |
XM_006724036.2 | 3028 | Missense Mutation | CCG,TCG | P857S | XP_006724099.1 |
XM_017028415.1 | 3028 | Missense Mutation | CCG,TCG | P882S | XP_016883904.1 |
XM_017028416.1 | 3028 | Missense Mutation | CCG,TCG | P860S | XP_016883905.1 |
XM_017028417.1 | 3028 | Missense Mutation | CCG,TCG | P802S | XP_016883906.1 |