| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001252020.1 | 4867 | Missense Mutation | CAC,CGC | H1518R | NP_001238949.1 |
| NM_001252024.1 | 4867 | Missense Mutation | CAC,CGC | H1501R | NP_001238953.1 |
| NM_001252030.1 | 4867 | Intron | NP_001238959.1 | ||
| NM_002420.5 | 4867 | Missense Mutation | CAC,CGC | H1479R | NP_002411.3 |