| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_007021.3 | 910 | Missense Mutation | CCG,CTG | P207L | NP_008952.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_032023.3 | 910 | Intron | NP_114412.2 | ||
| XM_005271833.4 | 910 | Intron | XP_005271890.1 | ||
| XM_005271835.4 | 910 | Intron | XP_005271892.1 | ||
| XM_006718013.3 | 910 | Intron | XP_006718076.1 | ||
| XM_006718014.3 | 910 | Intron | XP_006718077.1 | ||
| XM_011540255.2 | 910 | Intron | XP_011538557.1 | ||
| XM_017016754.1 | 910 | Intron | XP_016872243.1 | ||
| XM_017016755.1 | 910 | Intron | XP_016872244.1 | ||
| XM_017016756.1 | 910 | Intron | XP_016872245.1 | ||
| XM_017016757.1 | 910 | Intron | XP_016872246.1 | ||
| XM_017016758.1 | 910 | Intron | XP_016872247.1 |