| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001137604.2 | 237 | Missense Mutation | CCT,TCT | P3S | NP_001131076.1 |
| NM_001282772.1 | 237 | Missense Mutation | CCT,TCT | P41S | NP_001269701.1 |
| NM_001282774.1 | 237 | Missense Mutation | CCT,TCT | P3S | NP_001269703.1 |
| NM_001282776.1 | 237 | UTR 5 | NP_001269705.1 | ||
| NM_001282777.1 | 237 | UTR 5 | NP_001269706.1 | ||
| NM_001282779.1 | 237 | UTR 5 | NP_001269708.1 | ||
| NM_019014.5 | 237 | Missense Mutation | CCT,TCT | P3S | NP_061887.2 |