| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_002308.3 | 435 | Intron | NP_002299.2 | ||
| NM_009587.2 | 435 | Intron | NP_033665.1 | ||
| XM_006721892.2 | 435 | Intron | XP_006721955.1 | ||
| XM_006721893.2 | 435 | Intron | XP_006721956.1 | ||
| XM_006721894.3 | 435 | Intron | XP_006721957.1 | ||
| XM_006721895.3 | 435 | Intron | XP_006721958.1 | ||
| XM_011524796.1 | 435 | Missense Mutation | AAT,GAT | N109D | XP_011523098.1 |
| XM_017024623.1 | 435 | Intron | XP_016880112.1 |