| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000047.2 | 1438 | Intron | NP_000038.2 | ||
| NM_001282628.1 | 1438 | Intron | NP_001269557.1 | ||
| NM_001282631.1 | 1438 | Missense Mutation | AAA,ACA | K428T | NP_001269560.1 |
| XM_005274518.2 | 1438 | Intron | XP_005274575.1 | ||
| XM_005274519.4 | 1438 | Intron | XP_005274576.1 | ||
| XM_005274521.4 | 1438 | Intron | XP_005274578.1 | ||
| XM_011545521.1 | 1438 | Intron | XP_011543823.1 | ||
| XM_017029525.1 | 1438 | Intron | XP_016885014.1 | ||
| XM_017029526.1 | 1438 | Intron | XP_016885015.1 |