| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001160417.1 | 1152 | Missense Mutation | CGT,TGT | R365C | NP_001153889.1 |
| NM_001160418.1 | 1152 | Missense Mutation | CGT,TGT | R291C | NP_001153890.1 |
| NM_001160419.2 | 1152 | Intron | NP_001153891.1 | ||
| NM_001323966.1 | 1152 | Intron | NP_001310895.1 | ||
| NM_030776.2 | 1152 | Missense Mutation | CGT,TGT | R366C | NP_110403.2 |
| XM_011529057.2 | 1152 | Intron | XP_011527359.1 | ||
| XM_011529058.2 | 1152 | Intron | XP_011527360.1 | ||
| XM_017028086.1 | 1152 | Intron | XP_016883575.1 |