| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001290263.1 | 6830 | Missense Mutation | TAC,TGC | Y2158C | NP_001277192.1 |
| NM_014689.2 | 6830 | Missense Mutation | TAC,TGC | Y2164C | NP_055504.2 |
| XM_005246673.4 | 6830 | Missense Mutation | TAC,TGC | Y2177C | XP_005246730.1 |
| XM_006712617.3 | 6830 | Silent Mutation | CTA,CTG | L2202L | XP_006712680.1 |
| XM_017004441.1 | 6830 | Intron | XP_016859930.1 | ||
| XM_017004442.1 | 6830 | Intron | XP_016859931.1 | ||
| XM_017004443.1 | 6830 | Intron | XP_016859932.1 | ||
| XM_017004444.1 | 6830 | Intron | XP_016859933.1 | ||
| XM_017004445.1 | 6830 | Intron | XP_016859934.1 | ||
| XM_017004446.1 | 6830 | Intron | XP_016859935.1 | ||
| XM_017004447.1 | 6830 | Silent Mutation | CTA,CTG | L2193L | XP_016859936.1 |