| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001293.2 | 592 | Intron | NP_001284.1 | ||
| NM_001311199.1 | 592 | Missense Mutation | TCT,TTT | S167F | NP_001298128.1 |
| NM_001311200.1 | 592 | Intron | NP_001298129.1 | ||
| NM_001311201.1 | 592 | Intron | NP_001298130.1 | ||
| NM_001311202.1 | 592 | Intron | NP_001298131.1 |