| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001077628.2 | 382 | Intron | NP_001071096.1 | ||
| NM_001243771.1 | 382 | Intron | NP_001230700.1 | ||
| NM_001243772.1 | 382 | Intron | NP_001230701.1 | ||
| NM_016022.3 | 382 | Intron | NP_057106.2 | ||
| XM_017001417.1 | 382 | Intron | XP_016856906.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001301039.1 | 382 | Missense Mutation | AAT,ATT | N78I | NP_001287968.1 |
| NM_001301040.1 | 382 | Missense Mutation | AAT,ATT | N78I | NP_001287969.1 |
| NM_001301041.1 | 382 | Missense Mutation | AAT,ATT | N50I | NP_001287970.1 |
| NM_001301042.1 | 382 | Missense Mutation | AAT,ATT | N78I | NP_001287971.1 |
| NM_024579.3 | 382 | Missense Mutation | AAT,ATT | N78I | NP_078855.2 |
| XM_011509984.2 | 382 | Missense Mutation | AAT,ATT | N50I | XP_011508286.1 |