| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_022746.3 | 292 | Missense Mutation | CAC,CTC | H15L | NP_073583.3 |
| XM_011509900.2 | 292 | Missense Mutation | CAC,CTC | H15L | XP_011508202.1 |
| XM_011509903.2 | 292 | Intron | XP_011508205.1 | ||
| XM_011509904.2 | 292 | Intron | XP_011508206.1 | ||
| XM_017002096.1 | 292 | Intron | XP_016857585.1 | ||
| XM_017002097.1 | 292 | Intron | XP_016857586.1 |