| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001256648.1 | 6089 | Intron | NP_001243577.1 | ||
| NM_001256649.1 | 6089 | Missense Mutation | TGC,TGG | C81W | NP_001243578.1 |
| NM_001256650.1 | 6089 | Intron | NP_001243579.1 | ||
| NM_001256651.1 | 6089 | Intron | NP_001243580.1 | ||
| NM_001256653.1 | 6089 | Intron | NP_001243582.1 | ||
| NM_001256654.1 | 6089 | Missense Mutation | TGC,TGG | C22W | NP_001243583.1 |
| NM_003423.3 | 6089 | Missense Mutation | TGC,TGG | C87W | NP_003414.2 |
| XM_011528257.2 | 6089 | Intron | XP_011526559.1 | ||
| XM_011528259.2 | 6089 | Missense Mutation | TGC,TGG | C81W | XP_011526561.1 |
| XM_017027207.1 | 6089 | Intron | XP_016882696.1 | ||
| XM_017027208.1 | 6089 | Intron | XP_016882697.1 | ||
| XM_017027209.1 | 6089 | Intron | XP_016882698.1 | ||
| XM_017027210.1 | 6089 | Intron | XP_016882699.1 | ||
| XM_017027211.1 | 6089 | Missense Mutation | TGC,TGG | C81W | XP_016882700.1 |
| XM_017027212.1 | 6089 | Intron | XP_016882701.1 | ||
| XM_017027213.1 | 6089 | Intron | XP_016882702.1 | ||
| XM_017027214.1 | 6089 | Intron | XP_016882703.1 | ||
| XM_017027215.1 | 6089 | Intron | XP_016882704.1 | ||
| XM_017027216.1 | 6089 | Intron | XP_016882705.1 |