| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001304829.1 | 109 | Intron | NP_001291758.1 | ||
| NM_194292.2 | 109 | Intron | NP_919268.1 | ||
| XM_017000486.1 | 109 | Intron | XP_016855975.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_019083.2 | 109 | Missense Mutation | TCG,TTG | S7L | NP_061956.2 |
| XM_005270945.3 | 109 | Missense Mutation | TCG,TTG | S7L | XP_005271002.1 |
| XM_005270946.2 | 109 | UTR 5 | XP_005271003.1 | ||
| XM_017001504.1 | 109 | Missense Mutation | TCG,TTG | S7L | XP_016856993.1 |
| XM_017001505.1 | 109 | Missense Mutation | TCG,TTG | S7L | XP_016856994.1 |