| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001278596.1 | 8596 | Intron | NP_001265525.1 | ||
| NM_001278597.1 | 8596 | Intron | NP_001265526.1 | ||
| XM_006718988.3 | 8596 | Intron | XP_006719051.1 | ||
| XM_011520975.2 | 8596 | Intron | XP_011519277.1 | ||
| XM_011520978.2 | 8596 | Intron | XP_011519280.1 | ||
| XM_017019672.1 | 8596 | Intron | XP_016875161.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000552.4 | 8596 | Missense Mutation | CCC,TCC | P2781S | NP_000543.2 |