| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_013358.2 | 112 | Missense Mutation | GCT,GTT | A6V | NP_037490.2 |
| XM_011541307.1 | 112 | Missense Mutation | GCT,GTT | A6V | XP_011539609.1 |
| XM_017001101.1 | 112 | Intron | XP_016856590.1 | ||
| XM_017001102.1 | 112 | Intron | XP_016856591.1 | ||
| XM_017001103.1 | 112 | Missense Mutation | GCT,GTT | A6V | XP_016856592.1 |