| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001178075.1 | 1516 | Intron | NP_001171546.1 | ||
| NM_001178076.1 | 1516 | Intron | NP_001171547.1 | ||
| NM_001178077.1 | 1516 | Missense Mutation | CAT,CCT | H464P | NP_001171548.1 |
| NM_001673.4 | 1516 | Intron | NP_001664.3 | ||
| NM_133436.3 | 1516 | Missense Mutation | CAT,CCT | H547P | NP_597680.2 |
| NM_183356.3 | 1516 | Intron | NP_899199.2 |