Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001276468.1 | 1817 | Intron | NP_001263397.1 | ||
NM_001276469.1 | 1817 | Intron | NP_001263398.1 | ||
NM_001478.4 | 1817 | Intron | NP_001469.1 | ||
XM_005268773.4 | 1817 | UTR 3 | XP_005268830.1 | ||
XM_011538147.2 | 1817 | UTR 3 | XP_011536449.1 | ||
XM_011538148.2 | 1817 | UTR 3 | XP_011536450.1 | ||
XM_017019140.1 | 1817 | UTR 3 | XP_016874629.1 | ||
XM_017019141.1 | 1817 | UTR 3 | XP_016874630.1 | ||
XM_017019142.1 | 1817 | UTR 3 | XP_016874631.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_133489.2 | 1817 | Silent Mutation | CGC,CGG | R502R | NP_597996.2 |