Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001099681.2 | 531 | Intron | NP_001093151.2 | ||
NM_001099682.2 | 531 | Intron | NP_001093152.2 | ||
NM_024859.3 | 531 | Missense Mutation | AGG,GGG | R155G | NP_079135.3 |
XM_005278062.4 | 531 | Missense Mutation | AGG,GGG | R140G | XP_005278119.1 |
XM_005278063.4 | 531 | Missense Mutation | AGG,GGG | R140G | XP_005278120.1 |
XM_005278064.4 | 531 | Missense Mutation | AGG,GGG | R96G | XP_005278121.1 |
XM_005278065.3 | 531 | Missense Mutation | AGG,GGG | R96G | XP_005278122.1 |
XM_006724560.3 | 531 | Missense Mutation | AGG,GGG | R155G | XP_006724623.1 |
XM_011543985.2 | 531 | Missense Mutation | AGG,GGG | R96G | XP_011542287.1 |
XM_011543986.2 | 531 | Missense Mutation | AGG,GGG | R96G | XP_011542288.1 |
XM_011543987.2 | 531 | Missense Mutation | AGG,GGG | R96G | XP_011542289.1 |