Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_031471.5 | 442 | Missense Mutation | CAG,CGG | Q98R | NP_113659.3 |
NM_178443.2 | 442 | Missense Mutation | CAG,CGG | Q98R | NP_848537.1 |
XM_011545294.2 | 442 | Missense Mutation | CAG,CGG | Q98R | XP_011543596.1 |
XM_011545295.2 | 442 | UTR 5 | XP_011543597.1 | ||
XM_017018398.1 | 442 | Missense Mutation | CAG,CGG | Q98R | XP_016873887.1 |
XM_017018399.1 | 442 | UTR 5 | XP_016873888.1 |