| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_013379.2 | 1361 | Missense Mutation | CAC,CCC | H444P | NP_037511.2 |
| XM_005266075.3 | 1361 | Missense Mutation | CAC,CCC | H517P | XP_005266132.1 |
| XM_006717083.3 | 1361 | Silent Mutation | CCA,CCC | P494P | XP_006717146.1 |
| XM_011518599.2 | 1361 | Missense Mutation | CAC,CCC | H466P | XP_011516901.1 |
| XM_011518600.1 | 1361 | Missense Mutation | CAC,CCC | H436P | XP_011516902.1 |
| XM_017014651.1 | 1361 | Silent Mutation | CCA,CCC | P443P | XP_016870140.1 |
| XM_017014652.1 | 1361 | Silent Mutation | CCA,CCC | P421P | XP_016870141.1 |