| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_152353.2 | 1096 | Intron | NP_689566.1 | ||
| XM_011526425.2 | 1096 | Intron | XP_011524727.1 | ||
| XM_011526428.2 | 1096 | Intron | XP_011524730.1 | ||
| XM_017026244.1 | 1096 | Intron | XP_016881733.1 | ||
| XM_017026245.1 | 1096 | Intron | XP_016881734.1 | ||
| XM_017026246.1 | 1096 | Missense Mutation | ACA,GCA | T140A | XP_016881735.1 |
| XM_017026247.1 | 1096 | Intron | XP_016881736.1 |