| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001317958.1 | 1099 | Missense Mutation | CAG,CGG | Q184R | NP_001304887.1 |
| NM_001317959.1 | 1099 | Missense Mutation | CAG,CGG | Q216R | NP_001304888.1 |
| NM_152572.2 | 1099 | Missense Mutation | CAG,CGG | Q388R | NP_689785.1 |
| XM_005272169.2 | 1099 | Missense Mutation | CAG,CGG | Q400R | XP_005272226.1 |
| XM_006716965.2 | 1099 | Missense Mutation | CAG,CGG | Q316R | XP_006717028.1 |
| XM_011518277.2 | 1099 | Intron | XP_011516579.1 | ||
| XM_011518278.2 | 1099 | Missense Mutation | CAG,CGG | Q314R | XP_011516580.1 |
| XM_017014308.1 | 1099 | Missense Mutation | CAG,CGG | Q216R | XP_016869797.1 |