| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001206559.1 | 1374 | Intron | NP_001193488.1 | ||
| NM_015972.3 | 1374 | Missense Mutation | GCG,GTG | A110V | NP_057056.1 |
| NM_152705.2 | 1374 | Intron | NP_689918.1 | ||
| XM_005266412.1 | 1374 | Missense Mutation | GCG,GTG | A110V | XP_005266469.1 |
| XM_005266414.2 | 1374 | Intron | XP_005266471.1 | ||
| XM_017020622.1 | 1374 | Intron | XP_016876111.1 | ||
| XM_017020623.1 | 1374 | Intron | XP_016876112.1 |