| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001286732.1 | 2291 | Intron | NP_001273661.1 | ||
| NM_001286733.1 | 2291 | Missense Mutation | CCG,CTG | P205L | NP_001273662.1 |
| NM_024719.3 | 2291 | Missense Mutation | CGC,TGC | R325C | NP_078995.2 |
| XM_005268333.3 | 2291 | UTR 3 | XP_005268390.1 | ||
| XM_011537521.2 | 2291 | Intron | XP_011535823.1 | ||
| XM_011537522.2 | 2291 | Intron | XP_011535824.1 | ||
| XM_017020755.1 | 2291 | UTR 3 | XP_016876244.1 | ||
| XM_017020756.1 | 2291 | UTR 3 | XP_016876245.1 |