| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001300938.1 | 208 | UTR 5 | NP_001287867.1 | ||
| NM_001300939.1 | 208 | UTR 5 | NP_001287868.1 | ||
| NM_058244.3 | 208 | Missense Mutation | CTG,GTG | L4V | NP_490645.1 |
| XM_011543625.2 | 208 | Intron | XP_011541927.2 | ||
| XM_017009824.1 | 208 | Intron | XP_016865313.1 | ||
| XM_017009825.1 | 208 | Intron | XP_016865314.1 | ||
| XM_017009826.1 | 208 | Intron | XP_016865315.1 |