| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001271840.1 | 2048 | Missense Mutation | AAC,CAC | N417H | NP_001258769.1 |
| XM_006717947.3 | 2048 | Missense Mutation | AAC,CAC | N417H | XP_006718010.1 |
| XM_017016550.1 | 2048 | Missense Mutation | AAC,CAC | N417H | XP_016872039.1 |
| XM_017016551.1 | 2048 | Missense Mutation | AAC,CAC | N417H | XP_016872040.1 |
| XM_017016552.1 | 2048 | Missense Mutation | AAC,CAC | N417H | XP_016872041.1 |
| XM_017016553.1 | 2048 | Missense Mutation | AAC,CAC | N349H | XP_016872042.1 |
| XM_017016554.1 | 2048 | Missense Mutation | AAC,CAC | N349H | XP_016872043.1 |
| XM_017016555.1 | 2048 | Missense Mutation | AAC,CAC | N349H | XP_016872044.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_153336.2 | 2048 | Intron | NP_699167.2 | ||
| XM_017015640.1 | 2048 | Intron | XP_016871129.1 | ||
| XM_017015641.1 | 2048 | Intron | XP_016871130.1 |