Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_021615.4 | 1838 | Missense Mutation | CGG,CTG | R348L | NP_067628.1 |
XM_005255955.4 | 1838 | Missense Mutation | CGG,CTG | R348L | XP_005256012.1 |
XM_011523085.2 | 1838 | Missense Mutation | CGG,CTG | R348L | XP_011521387.1 |