| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001077349.1 | 601 | Intron | NP_001070817.1 | ||
| NM_033196.2 | 601 | Intron | NP_149973.1 | ||
| XM_017027455.1 | 601 | Missense Mutation | GAT,GGT | D131G | XP_016882944.1 |
| XM_017027456.1 | 601 | Intron | XP_016882945.1 |