Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001145125.1 | 1249 | Intron | NP_001138597.1 | ||
NM_001291663.1 | 1249 | Intron | NP_001278592.1 | ||
NM_013446.3 | 1249 | Missense Mutation | CCG,CGG | P412R | NP_038474.2 |
XM_011515996.1 | 1249 | Missense Mutation | CCG,CGG | P369R | XP_011514298.1 |
XM_011515997.2 | 1249 | Missense Mutation | CCG,CGG | P348R | XP_011514299.1 |
XM_011515998.1 | 1249 | Intron | XP_011514300.1 |