| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001099439.1 | 2982 | Missense Mutation | GCC,TCC | A966S | NP_001092909.1 |
| NM_173641.2 | 2982 | Intron | NP_775912.2 | ||
| XM_017001080.1 | 2982 | Missense Mutation | GCC,TCC | A569S | XP_016856569.1 |
| XM_017001081.1 | 2982 | Missense Mutation | GGC,GTC | G571V | XP_016856570.1 |