| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001271667.1 | 1088 | Intron | NP_001258596.1 | ||
| NM_001271668.1 | 1088 | Intron | NP_001258597.1 | ||
| NM_001271669.1 | 1088 | Intron | NP_001258598.1 | ||
| NM_032122.4 | 1088 | Intron | NP_115498.2 | ||
| NM_183040.2 | 1088 | Missense Mutation | GCC,GTC | A300V | NP_898861.1 |
| XM_005249447.4 | 1088 | Intron | XP_005249504.1 | ||
| XM_011514936.2 | 1088 | Intron | XP_011513238.1 | ||
| XM_011514937.2 | 1088 | Intron | XP_011513239.1 | ||
| XM_017011348.1 | 1088 | Intron | XP_016866837.1 | ||
| XM_017011349.1 | 1088 | Intron | XP_016866838.1 |