| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001102657.1 | 2978 | Missense Mutation | ACT,GCT | T857A | NP_001096127.1 |
| XM_011526558.2 | 2978 | Missense Mutation | ACT,GCT | T857A | XP_011524860.1 |
| XM_011526559.2 | 2978 | Missense Mutation | ACT,GCT | T857A | XP_011524861.1 |
| XM_017026389.1 | 2978 | Intron | XP_016881878.1 |