| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001300796.1 | 262 | Intron | NP_001287725.1 | ||
| NM_001300797.1 | 262 | Intron | NP_001287726.1 | ||
| NM_006325.4 | 262 | Missense Mutation | ACT,GCT | T2A | NP_006316.1 |
| XM_017019772.1 | 262 | Missense Mutation | ACT,GCT | T2A | XP_016875261.1 |
| XM_017019773.1 | 262 | Intron | XP_016875262.1 |