| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001039707.1 | 922 | Intron | NP_001034796.1 | ||
| NM_001039708.1 | 922 | Intron | NP_001034797.1 | ||
| NM_006643.3 | 922 | Intron | NP_006634.3 | ||
| XM_005266050.3 | 922 | Intron | XP_005266107.1 | ||
| XM_005266051.3 | 922 | Intron | XP_005266108.1 | ||
| XM_011518157.2 | 922 | Missense Mutation | ATC,ATG | I278M | XP_011516459.1 |
| XM_017014218.1 | 922 | Intron | XP_016869707.1 | ||
| XM_017014219.1 | 922 | Intron | XP_016869708.1 |