Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001130028.1 | 1688 | Intron | NP_001123500.1 | ||
NM_003992.4 | 1688 | Intron | NP_003983.2 | ||
XM_005254151.3 | 1688 | Intron | XP_005254208.1 | ||
XM_011521205.2 | 1688 | Intron | XP_011519507.1 | ||
XM_011521206.2 | 1688 | Intron | XP_011519508.1 | ||
XM_011521209.2 | 1688 | Intron | XP_011519511.2 | ||
XM_017021905.1 | 1688 | Intron | XP_016877394.1 | ||
XM_017021906.1 | 1688 | Intron | XP_016877395.1 | ||
XM_017021907.1 | 1688 | Intron | XP_016877396.1 | ||
XM_017021908.1 | 1688 | Intron | XP_016877397.1 | ||
XM_017021909.1 | 1688 | Intron | XP_016877398.1 | ||
XM_017021910.1 | 1688 | Intron | XP_016877399.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001142443.1 | 1688 | Missense Mutation | GAC,GGC | D472G | NP_001135915.1 |
NM_001142444.1 | 1688 | Missense Mutation | GAC,GGC | D472G | NP_001135916.1 |
NM_025083.3 | 1688 | Missense Mutation | GAC,GGC | D472G | NP_079359.2 |
XM_011522092.2 | 1688 | Missense Mutation | GAC,GGC | D289G | XP_011520394.1 |