| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001160223.1 | 683 | Intron | NP_001153695.1 | ||
| NM_001160224.1 | 683 | Missense Mutation | AAT,CAT | N146H | NP_001153696.1 |
| NM_001160225.1 | 683 | Intron | NP_001153697.1 | ||
| NM_030954.3 | 683 | Intron | NP_112216.3 | ||
| XM_006716404.2 | 683 | Intron | XP_006716467.1 | ||
| XM_006716405.2 | 683 | Intron | XP_006716468.1 | ||
| XM_011544666.2 | 683 | Intron | XP_011542968.1 | ||
| XM_017013881.1 | 683 | Intron | XP_016869370.1 | ||
| XM_017013882.1 | 683 | Intron | XP_016869371.1 |