| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001195833.1 | 1242 | Intron | NP_001182762.1 | ||
| NM_198445.3 | 1242 | Intron | NP_940847.1 | ||
| XM_006723015.2 | 1242 | Intron | XP_006723078.1 | ||
| XM_006723016.2 | 1242 | Intron | XP_006723079.1 | ||
| XM_011526454.2 | 1242 | Intron | XP_011524756.1 | ||
| XM_011526455.2 | 1242 | Intron | XP_011524757.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001193286.1 | 1242 | UTR 3 | NP_001180215.1 | ||
| NM_012237.3 | 1242 | Missense Mutation | ACA,ATA | T352I | NP_036369.2 |
| NM_030593.2 | 1242 | Missense Mutation | ACA,ATA | T315I | NP_085096.1 |
| XM_006723111.1 | 1242 | Missense Mutation | ACA,ATA | T315I | XP_006723174.1 |
| XM_011526654.1 | 1242 | Missense Mutation | ACA,ATA | T315I | XP_011524956.1 |
| XM_011526655.1 | 1242 | Missense Mutation | ACA,ATA | T282I | XP_011524957.1 |
| XM_017026500.1 | 1242 | Missense Mutation | ACA,ATA | T229I | XP_016881989.1 |