| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001287489.1 | 3885 | Missense Mutation | CCT,CGT | P1987R | NP_001274418.1 |
| NM_004802.3 | 3885 | UTR 3 | NP_004793.2 | ||
| NM_194248.2 | 3885 | UTR 3 | NP_919224.1 | ||
| NM_194322.2 | 3885 | UTR 3 | NP_919303.1 | ||
| NM_194323.2 | 3885 | Missense Mutation | CCT,CGT | P1220R | NP_919304.1 |
| XM_017005338.1 | 3885 | Intron | XP_016860827.1 |