| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001122823.1 | 472 | Silent Mutation | GGC,GGT | G45G | NP_001116295.1 |
| NM_001286709.1 | 472 | Missense Mutation | GCG,GTG | A11V | NP_001273638.1 |
| NM_012087.3 | 472 | Silent Mutation | GGC,GGT | G45G | NP_036219.2 |
| XM_005272234.3 | 472 | Silent Mutation | GGC,GGT | G45G | XP_005272291.1 |
| XM_011519201.1 | 472 | Intron | XP_011517503.1 | ||
| XM_017015315.1 | 472 | Intron | XP_016870804.1 | ||
| XM_017015316.1 | 472 | Intron | XP_016870805.1 |