| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001010978.3 | 239 | Silent Mutation | GGC,GGT | G98G | NP_001010978.2 |
| NM_001276392.1 | 239 | Silent Mutation | GGC,GGT | G59G | NP_001263321.1 |
| NM_001276393.1 | 239 | Silent Mutation | GGC,GGT | G55G | NP_001263322.1 |
| NM_001276394.1 | 239 | Intron | NP_001263323.1 | ||
| NM_001276395.1 | 239 | Missense Mutation | GCG,GTG | A45V | NP_001263324.1 |
| XM_011541446.1 | 239 | Silent Mutation | GGC,GGT | G97G | XP_011539748.1 |
| XM_017001264.1 | 239 | Missense Mutation | GCG,GTG | A45V | XP_016856753.1 |