Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_006293.3 | 480 | Missense Mutation | CGG,CTG | R148L | NP_006284.2 |
XM_017022542.1 | 480 | Missense Mutation | CGG,CTG | R103L | XP_016878031.1 |
XM_017022543.1 | 480 | Missense Mutation | CGG,CTG | R148L | XP_016878032.1 |