| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001283056.1 | 840 | Missense Mutation | GCC,GGC | A231G | NP_001269985.1 |
| NM_001283057.1 | 840 | Intron | NP_001269986.1 | ||
| NM_001283058.1 | 840 | Intron | NP_001269987.1 | ||
| NM_001283059.1 | 840 | Intron | NP_001269988.1 | ||
| NM_001283060.1 | 840 | Intron | NP_001269989.1 | ||
| NM_018168.3 | 840 | Intron | NP_060638.2 | ||
| XM_005267806.1 | 840 | Missense Mutation | GCC,GGC | A232G | XP_005267863.1 |
| XM_005267810.3 | 840 | Intron | XP_005267867.1 | ||
| XM_005267811.3 | 840 | Intron | XP_005267868.1 | ||
| XM_005267813.1 | 840 | Intron | XP_005267870.1 | ||
| XM_005267814.1 | 840 | Intron | XP_005267871.1 | ||
| XM_006720188.2 | 840 | Intron | XP_006720251.1 | ||
| XM_006720189.2 | 840 | Intron | XP_006720252.1 |