Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001077365.1 | 268 | Silent Mutation | CTG,CTT | L22L | NP_001070833.1 |
NM_001077366.1 | 268 | Intron | NP_001070834.1 | ||
NM_001136113.1 | 268 | Silent Mutation | CTG,CTT | L22L | NP_001129585.1 |
NM_001136114.1 | 268 | Intron | NP_001129586.1 | ||
NM_007171.3 | 268 | Silent Mutation | CTG,CTT | L22L | NP_009102.3 |
XM_005272156.1 | 268 | Silent Mutation | CTG,CTT | L22L | XP_005272213.1 |
XM_005272158.1 | 268 | Intron | XP_005272215.1 | ||
XM_005272159.1 | 268 | Intron | XP_005272216.1 | ||
XM_005272162.2 | 268 | UTR 5 | XP_005272219.1 | ||
XM_006716932.1 | 268 | UTR 5 | XP_006716995.1 | ||
XM_011518140.1 | 268 | Silent Mutation | CTG,CTT | L22L | XP_011516442.1 |
XM_011518141.1 | 268 | Silent Mutation | CTG,CTT | L22L | XP_011516443.1 |
XM_011518142.1 | 268 | Intron | XP_011516444.1 | ||
XM_011518143.1 | 268 | Silent Mutation | CTG,CTT | L22L | XP_011516445.1 |
XM_011518145.1 | 268 | Intron | XP_011516447.1 | ||
XM_017014203.1 | 268 | UTR 5 | XP_016869692.1 | ||
XM_017014204.1 | 268 | Intron | XP_016869693.1 | ||
XM_017014205.1 | 268 | UTR 5 | XP_016869694.1 |