Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_178517.3 | 619 | Missense Mutation | CGG,CTG | R107L | NP_848612.2 |
XM_005257238.2 | 619 | Missense Mutation | CGG,CTG | R107L | XP_005257295.1 |
XM_011524646.2 | 619 | Missense Mutation | CGG,CTG | R107L | XP_011522948.1 |