| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001277813.1 | 451 | Missense Mutation | AAG,CAG | K48Q | NP_001264742.1 |
| NM_001277814.1 | 451 | Missense Mutation | AAG,CAG | K48Q | NP_001264743.1 |
| NM_001277815.1 | 451 | UTR 5 | NP_001264744.1 | ||
| NM_001277816.1 | 451 | Intron | NP_001264745.1 | ||
| NM_001277817.1 | 451 | UTR 5 | NP_001264746.1 | ||
| NM_001277818.1 | 451 | UTR 5 | NP_001264747.1 | ||
| NM_152758.5 | 451 | Missense Mutation | AAG,CAG | K45Q | NP_689971.4 |
| XM_011517509.2 | 451 | Missense Mutation | AAG,CAG | K48Q | XP_011515811.1 |
| XM_011517510.2 | 451 | Intron | XP_011515812.1 |