| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001135998.2 | 605 | Missense Mutation | GCC,GTC | A25V | NP_001129470.1 |
| NM_019056.6 | 605 | Missense Mutation | GCC,GTC | A25V | NP_061929.2 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001204466.1 | 605 | Intron | NP_001191395.1 | ||
| NM_001204467.1 | 605 | Intron | NP_001191396.1 | ||
| NM_001204468.1 | 605 | Intron | NP_001191397.1 | ||
| NM_005676.4 | 605 | Intron | NP_005667.2 | ||
| NM_152856.2 | 605 | Intron | NP_690595.1 | ||
| XM_005272677.4 | 605 | Intron | XP_005272734.1 | ||
| XM_005272678.4 | 605 | Intron | XP_005272735.1 | ||
| XM_005272679.4 | 605 | Intron | XP_005272736.1 | ||
| XM_006724563.1 | 605 | Intron | XP_006724626.1 | ||
| XM_011543989.2 | 605 | Intron | XP_011542291.1 | ||
| XM_017029884.1 | 605 | Intron | XP_016885373.1 | ||
| XM_017029885.1 | 605 | Intron | XP_016885374.1 |