Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001316963.1 | 651 | Missense Mutation | CAG,CGG | Q97R | NP_001303892.1 |
NM_001729.3 | 651 | Missense Mutation | CAG,CGG | Q146R | NP_001720.1 |
XM_011532211.1 | 651 | Missense Mutation | CAG,CGG | Q146R | XP_011530513.1 |
XM_017008568.1 | 651 | Intron | XP_016864057.1 |