Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001195736.1 | 2762 | UTR 3 | NP_001182665.1 | ||
NM_001195737.1 | 2762 | UTR 3 | NP_001182666.1 | ||
NM_001195738.1 | 2762 | UTR 3 | NP_001182667.1 | ||
NM_001195740.1 | 2762 | UTR 3 | NP_001182669.1 | ||
NM_001195741.1 | 2762 | UTR 3 | NP_001182670.1 | ||
NM_152371.3 | 2762 | UTR 3 | NP_689584.2 | ||
XM_006710354.3 | 2762 | UTR 3 | XP_006710417.1 | ||
XM_011540664.1 | 2762 | UTR 3 | XP_011538966.1 | ||
XM_011540665.1 | 2762 | UTR 3 | XP_011538967.1 | ||
XM_011540666.1 | 2762 | UTR 3 | XP_011538968.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_033467.3 | 2762 | Missense Mutation | ACG,ATG | T761M | NP_258428.2 |
XM_011542122.2 | 2762 | Missense Mutation | ACG,ATG | T504M | XP_011540424.1 |
XM_017002310.1 | 2762 | Missense Mutation | ACG,ATG | T761M | XP_016857799.1 |
XM_017002311.1 | 2762 | Missense Mutation | ACG,ATG | T743M | XP_016857800.1 |
XM_017002312.1 | 2762 | Missense Mutation | ACG,ATG | T735M | XP_016857801.1 |
XM_017002313.1 | 2762 | Missense Mutation | ACG,ATG | T729M | XP_016857802.1 |
XM_017002314.1 | 2762 | Missense Mutation | ACG,ATG | T718M | XP_016857803.1 |
XM_017002315.1 | 2762 | Missense Mutation | ACG,ATG | T657M | XP_016857804.1 |