| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001033561.1 | 2924 | Intron | NP_001028733.1 | ||
| NM_001290131.1 | 2924 | Missense Mutation | AGA,AGC | R798S | NP_001277060.1 |
| NM_020889.2 | 2924 | Intron | NP_065940.1 | ||
| XM_005258015.3 | 2924 | Intron | XP_005258072.1 | ||
| XM_005258016.3 | 2924 | Intron | XP_005258073.1 | ||
| XM_011525078.2 | 2924 | Intron | XP_011523380.1 | ||
| XM_011525079.2 | 2924 | Intron | XP_011523381.1 | ||
| XM_011525082.2 | 2924 | Intron | XP_011523384.1 | ||
| XM_011525083.2 | 2924 | Intron | XP_011523385.1 | ||
| XM_017024903.1 | 2924 | Intron | XP_016880392.1 | ||
| XM_017024904.1 | 2924 | Intron | XP_016880393.1 |