| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001318189.1 | 298 | Missense Mutation | CGC,TGC | R14C | NP_001305118.1 |
| NM_144587.3 | 298 | Missense Mutation | CGC,TGC | R13C | NP_653188.2 |
| XM_011539239.2 | 298 | Missense Mutation | CGC,TGC | R14C | XP_011537541.1 |
| XM_011539240.2 | 298 | Missense Mutation | CGC,TGC | R14C | XP_011537542.1 |
| XM_011539241.2 | 298 | Missense Mutation | CGC,TGC | R14C | XP_011537543.1 |
| XM_011539242.2 | 298 | Missense Mutation | CGC,TGC | R14C | XP_011537544.1 |
| XM_017015636.1 | 298 | Missense Mutation | CGC,TGC | R14C | XP_016871125.1 |
| XM_017015637.1 | 298 | Intron | XP_016871126.1 |