| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001145166.1 | 465 | Intron | NP_001138638.1 | ||
| NM_001145167.1 | 465 | Missense Mutation | GAA,GGA | E6G | NP_001138639.1 |
| NM_005788.3 | 465 | Missense Mutation | GAA,GGA | E83G | NP_005779.1 |
| XM_011519836.2 | 465 | Intron | XP_011518138.1 | ||
| XM_017017081.1 | 465 | Intron | XP_016872570.1 |