| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_052934.3 | 2660 | UTR 3 | NP_443166.1 | ||
| NM_134325.2 | 2660 | Missense Mutation | CAA,CGA | Q849R | NP_599152.2 |
| XM_011509121.2 | 2660 | UTR 3 | XP_011507423.1 | ||
| XM_011509122.2 | 2660 | UTR 3 | XP_011507424.1 | ||
| XM_011509124.2 | 2660 | Intron | XP_011507426.1 |