| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001185099.1 | 368 | Missense Mutation | CGG,CTG | R95L | NP_001172028.1 |
| NM_001185100.1 | 368 | Missense Mutation | CGG,CTG | R95L | NP_001172029.1 |
| NM_001185101.1 | 368 | Missense Mutation | CGG,CTG | R95L | NP_001172030.1 |
| NM_001278417.1 | 368 | UTR 5 | NP_001265346.1 | ||
| NM_001771.3 | 368 | Missense Mutation | CGG,CTG | R95L | NP_001762.2 |