| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_213604.2 | 1469 | Missense Mutation | CGC,TGC | R388C | NP_998769.2 |
| XM_005259549.3 | 1469 | Missense Mutation | CGC,TGC | R398C | XP_005259606.1 |
| XM_011527961.1 | 1469 | Missense Mutation | CGC,TGC | R402C | XP_011526263.1 |
| XM_011527963.1 | 1469 | Missense Mutation | CGC,TGC | R157C | XP_011526265.1 |
| XM_017026744.1 | 1469 | Missense Mutation | CGC,TGC | R392C | XP_016882233.1 |
| XM_017026745.1 | 1469 | Missense Mutation | CGC,TGC | R388C | XP_016882234.1 |