Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001294340.1 | 373 | Missense Mutation | CCG,CTG | P58L | NP_001281269.1 |
NM_144604.3 | 373 | Missense Mutation | CCG,CTG | P58L | NP_653205.3 |
XM_011522863.1 | 373 | Missense Mutation | CCG,CTG | P58L | XP_011521165.1 |
XM_011522865.1 | 373 | Intron | XP_011521167.1 | ||
XM_017022934.1 | 373 | Missense Mutation | CCG,CTG | P58L | XP_016878423.1 |