Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_017870.3 | 798 | Missense Mutation | CGG,CTG | R202L | NP_060340.2 |
NM_178031.2 | 798 | Missense Mutation | CGG,CTG | R202L | NP_821174.1 |
XM_017017951.1 | 798 | Missense Mutation | CGG,CTG | R215L | XP_016873440.1 |
XM_017017952.1 | 798 | Missense Mutation | CGG,CTG | R215L | XP_016873441.1 |