| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001306153.1 | 466 | Missense Mutation | AAT,CAT | N51H | NP_001293082.1 |
| NM_001306154.1 | 466 | Intron | NP_001293083.1 | ||
| NM_001306155.1 | 466 | Intron | NP_001293084.1 | ||
| NM_001306156.1 | 466 | Missense Mutation | AAT,CAT | N34H | NP_001293085.1 |
| NM_012073.4 | 466 | Missense Mutation | AAT,CAT | N72H | NP_036205.1 |