Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001144952.1 | 6383 | Missense Mutation | CAG,CGG | Q2128R | NP_001138424.1 |
XM_011524914.2 | 6383 | Missense Mutation | CAG,CGG | Q2109R | XP_011523216.1 |
XM_011524915.2 | 6383 | Intron | XP_011523217.1 | ||
XM_011524916.2 | 6383 | Intron | XP_011523218.1 |