| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001113182.2 | 1327 | Missense Mutation | CAC,CCC | H8P | NP_001106653.1 |
| NM_001199455.1 | 1327 | Missense Mutation | CAC,CCC | H8P | NP_001186384.1 |
| NM_001199456.1 | 1327 | Intron | NP_001186385.1 | ||
| NM_001291986.1 | 1327 | UTR 5 | NP_001278915.1 | ||
| NM_005104.3 | 1327 | Missense Mutation | CAC,CCC | H8P | NP_005095.1 |