| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001143986.1 | 262 | Silent Mutation | AAC,AAT | N77N | NP_001137458.1 |
| NM_024760.2 | 262 | UTR 5 | NP_079036.1 | ||
| XM_005259645.2 | 262 | Silent Mutation | AAC,AAT | N77N | XP_005259702.1 |
| XM_011528300.2 | 262 | Missense Mutation | AAC,AAT | N77N | XP_011526602.1 |
| XM_011528301.1 | 262 | UTR 5 | XP_011526603.1 | ||
| XM_011528306.1 | 262 | UTR 5 | XP_011526608.1 |