Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001323956.1 | 554 | UTR 5 | NP_001310885.1 | ||
NM_001323958.1 | 554 | Intron | NP_001310887.1 | ||
NM_001323960.1 | 554 | Missense Mutation | CAA,CGA | Q17R | NP_001310889.1 |
NM_006462.5 | 554 | Intron | NP_006453.1 | ||
NM_031229.3 | 554 | Missense Mutation | CAA,CGA | Q17R | NP_112506.2 |
XM_005260645.1 | 554 | Missense Mutation | CAA,CGA | Q34R | XP_005260702.1 |
XM_011529137.1 | 554 | Missense Mutation | CAA,CGA | Q34R | XP_011527439.1 |
XM_011529138.1 | 554 | Missense Mutation | CAA,CGA | Q17R | XP_011527440.1 |
XM_011529139.2 | 554 | Missense Mutation | CAA,CGA | Q34R | XP_011527441.1 |
XM_011529140.1 | 554 | Missense Mutation | CAA,CGA | Q34R | XP_011527442.1 |
XM_017027594.1 | 554 | UTR 5 | XP_016883083.1 | ||
XM_017027595.1 | 554 | UTR 5 | XP_016883084.1 |