Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001184714.1 | 852 | Missense Mutation | CAA,CGA | Q261R | NP_001171643.1 |
NM_001184715.1 | 852 | Missense Mutation | CAA,CGA | Q212R | NP_001171644.1 |
NM_001184716.1 | 852 | Missense Mutation | CAA,CGA | Q150R | NP_001171645.1 |
NM_052931.4 | 852 | Missense Mutation | CAA,CGA | Q261R | NP_443163.1 |
XM_017000215.1 | 852 | Missense Mutation | CAA,CGA | Q261R | XP_016855704.1 |
XM_017000216.1 | 852 | Missense Mutation | CAA,CGA | Q212R | XP_016855705.1 |
XM_017000217.1 | 852 | Missense Mutation | CAA,CGA | Q150R | XP_016855706.1 |