Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001079528.3 | 4327 | Intron | NP_001072996.1 | ||
NM_001171.5 | 4327 | Silent Mutation | CTA,CTG | L1438L | NP_001162.4 |
XM_011522479.2 | 4327 | Silent Mutation | CTA,CTG | L1427L | XP_011520781.1 |
XM_011522480.1 | 4327 | Silent Mutation | CTA,CTG | L1324L | XP_011520782.1 |
XM_011522481.2 | 4327 | Silent Mutation | CTA,CTG | L1324L | XP_011520783.1 |
XM_011522482.2 | 4327 | Intron | XP_011520784.1 | ||
XM_017023212.1 | 4327 | Silent Mutation | CTA,CTG | L1382L | XP_016878701.1 |
XM_017023213.1 | 4327 | Silent Mutation | CTA,CTG | L1324L | XP_016878702.1 |
XM_017023214.1 | 4327 | Intron | XP_016878703.1 |