Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001001671.3 | 3136 | Missense Mutation | CCA,CTA | P1280L | NP_001001671.3 |
XM_011545507.2 | 3136 | Missense Mutation | CCA,CTA | P1291L | XP_011543809.2 |
XM_011545508.2 | 3136 | Missense Mutation | CCA,CTA | P1262L | XP_011543810.2 |
XM_011545510.2 | 3136 | Missense Mutation | CCA,CTA | P838L | XP_011543812.1 |
XM_011545511.2 | 3136 | Missense Mutation | CCA,CTA | P715L | XP_011543813.1 |
XM_017029511.1 | 3136 | Intron | XP_016885000.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000284.3 | 3136 | UTR 3 | NP_000275.1 | ||
NM_001173454.1 | 3136 | UTR 3 | NP_001166925.1 | ||
NM_001173455.1 | 3136 | UTR 3 | NP_001166926.1 | ||
NM_001173456.1 | 3136 | UTR 3 | NP_001166927.1 | ||
XM_017029574.1 | 3136 | Intron | XP_016885063.1 |