| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000889.2 | 2597 | Missense Mutation | CGC,TGC | R789C | NP_000880.1 |
| XM_005268851.3 | 2597 | Missense Mutation | CGC,TGC | R789C | XP_005268908.1 |
| XM_005268852.4 | 2597 | Missense Mutation | CGC,TGC | R789C | XP_005268909.1 |
| XM_006719376.3 | 2597 | UTR 3 | XP_006719439.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001004304.3 | 2597 | Intron | NP_001004304.1 | ||
| XM_006719344.2 | 2597 | Intron | XP_006719407.1 | ||
| XM_011538194.2 | 2597 | Intron | XP_011536496.1 | ||
| XM_017019181.1 | 2597 | Intron | XP_016874670.1 |