| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001288834.1 | 2436 | Intron | NP_001275763.1 | ||
| NM_032207.3 | 2436 | UTR 3 | NP_115583.1 | ||
| XM_006722920.3 | 2436 | UTR 3 | XP_006722983.1 | ||
| XM_011528354.2 | 2436 | Intron | XP_011526656.1 | ||
| XM_017027350.1 | 2436 | Intron | XP_016882839.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_006387.5 | 2436 | Missense Mutation | CGC,TGC | R788C | NP_006378.3 |