| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001304495.1 | 1478 | UTR 3 | NP_001291424.1 | ||
| NM_171982.4 | 1478 | Missense Mutation | CGC,TGC | R456C | NP_741983.2 |
| XM_005273452.3 | 1478 | UTR 3 | XP_005273509.1 | ||
| XM_011544453.1 | 1478 | Missense Mutation | CGC,TGC | R306C | XP_011542755.1 |