| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001007225.1 | 1354 | Intron | NP_001007226.1 | ||
| NM_001291869.1 | 1354 | Intron | NP_001278798.1 | ||
| NM_001291872.1 | 1354 | Intron | NP_001278801.1 | ||
| NM_001291873.1 | 1354 | Intron | NP_001278802.1 | ||
| NM_001291874.1 | 1354 | Intron | NP_001278803.1 | ||
| NM_001291875.1 | 1354 | Intron | NP_001278804.1 | ||
| NM_006548.4 | 1354 | Intron | NP_006539.3 | ||
| XM_006713477.3 | 1354 | Intron | XP_006713540.1 | ||
| XM_006713478.3 | 1354 | Intron | XP_006713541.1 | ||
| XM_017005557.1 | 1354 | Intron | XP_016861046.1 | ||
| XM_017005558.1 | 1354 | Intron | XP_016861047.1 | ||
| XM_017005559.1 | 1354 | Intron | XP_016861048.1 | ||
| XM_017005560.1 | 1354 | Intron | XP_016861049.1 | ||
| XM_017005561.1 | 1354 | Missense Mutation | CCG,CTG | P423L | XP_016861050.1 |
| XM_017005562.1 | 1354 | Intron | XP_016861051.1 | ||
| XM_017005563.1 | 1354 | Intron | XP_016861052.1 | ||
| XM_017005564.1 | 1354 | Intron | XP_016861053.1 |