Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001282766.1 | 291 | UTR 5 | NP_001269695.1 | ||
NM_022490.2 | 291 | Silent Mutation | CTG,TTG | L60L | NP_071935.1 |
XM_005251547.2 | 291 | Missense Mutation | CTG,TTG | L122L | XP_005251604.1 |