| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_021228.2 | 46 | Missense Mutation | CCT,CGT | P76R | NP_067051.2 |
| XM_005259122.4 | 46 | Missense Mutation | CCT,CGT | P76R | XP_005259179.1 |
| XM_011527194.2 | 46 | Missense Mutation | CCT,CGT | P79R | XP_011525496.1 |
| XM_017027083.1 | 46 | UTR 5 | XP_016882572.1 |