| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001142763.1 | 5121 | Intron | NP_001136235.1 | ||
| NM_001142764.1 | 5121 | Intron | NP_001136236.1 | ||
| NM_001142765.1 | 5121 | Intron | NP_001136237.1 | ||
| NM_001142766.1 | 5121 | Intron | NP_001136238.1 | ||
| NM_001142767.1 | 5121 | Intron | NP_001136239.1 | ||
| NM_001142768.1 | 5121 | Intron | NP_001136240.1 | ||
| NM_001142769.1 | 5121 | Intron | NP_001136241.1 | ||
| NM_001142770.1 | 5121 | Intron | NP_001136242.1 | ||
| NM_001142771.1 | 5121 | Missense Mutation | ACC,CCC | T1576P | NP_001136243.1 |
| NM_001142772.1 | 5121 | Missense Mutation | ACC,CCC | T1571P | NP_001136244.1 |
| NM_001142773.1 | 5121 | Intron | NP_001136245.1 | ||
| NM_033056.3 | 5121 | Intron | NP_149045.3 | ||
| XM_017016571.1 | 5121 | Missense Mutation | ACC,CCC | T1612P | XP_016872060.1 |
| XM_017016572.1 | 5121 | Missense Mutation | ACC,CCC | T1569P | XP_016872061.1 |
| XM_017016573.1 | 5121 | Intron | XP_016872062.1 |