| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001142270.1 | 147 | Intron | NP_001135742.1 | ||
| NM_001142271.1 | 147 | Intron | NP_001135743.1 | ||
| NM_001289763.1 | 147 | Missense Mutation | CAG,CGG | Q30R | NP_001276692.1 |
| NM_199204.1 | 147 | UTR 5 | NP_954674.1 | ||
| XM_011510475.1 | 147 | UTR 5 | XP_011508777.1 |