| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001033024.1 | 348 | Intron | NP_001028196.1 | ||
| NM_001257990.1 | 348 | Intron | NP_001244919.1 | ||
| NM_012179.3 | 348 | Missense Mutation | ACG,ATG | T22M | NP_036311.3 |
| XM_011530106.1 | 348 | UTR 5 | XP_011528408.1 |