| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001286703.1 | 353 | Intron | NP_001273632.1 | ||
| NM_001286704.1 | 353 | Missense Mutation | GCC,GGC | A29G | NP_001273633.1 |
| NM_001286705.1 | 353 | Intron | NP_001273634.1 | ||
| NM_001286706.1 | 353 | Intron | NP_001273635.1 | ||
| NM_016617.3 | 353 | Intron | NP_057701.1 |