Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001130071.1 | 289 | Missense Mutation | AGG,GGG | R91G | NP_001123543.1 |
NM_001130072.1 | 289 | UTR 5 | NP_001123544.1 | ||
NM_013333.3 | 289 | UTR 5 | NP_037465.2 | ||
XM_005258829.2 | 289 | UTR 5 | XP_005258886.1 | ||
XM_005258830.2 | 289 | UTR 5 | XP_005258887.1 | ||
XM_011526880.1 | 289 | UTR 5 | XP_011525182.1 | ||
XM_011526881.1 | 289 | UTR 5 | XP_011525183.1 | ||
XM_017026722.1 | 289 | UTR 5 | XP_016882211.1 | ||
XM_017026723.1 | 289 | Missense Mutation | AGG,GGG | R40G | XP_016882212.1 |
XM_017026724.1 | 289 | Missense Mutation | AGG,GGG | R40G | XP_016882213.1 |
XM_017026725.1 | 289 | Missense Mutation | AGG,GGG | R40G | XP_016882214.1 |