| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001193511.1 | 2730 | Missense Mutation | CCT,CTT | P844L | NP_001180440.1 |
| NM_006301.3 | 2730 | Missense Mutation | CCT,CTT | P811L | NP_006292.3 |
| XM_005269138.3 | 2730 | Missense Mutation | CCT,CTT | P844L | XP_005269195.1 |
| XM_005269140.2 | 2730 | Intron | XP_005269197.1 | ||
| XM_006719588.3 | 2730 | Missense Mutation | CCT,CTT | P844L | XP_006719651.1 |
| XM_011538725.2 | 2730 | Missense Mutation | CCT,CTT | P844L | XP_011537027.1 |
| XM_017019956.1 | 2730 | Missense Mutation | CCT,CTT | P811L | XP_016875445.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001098620.2 | 2730 | Intron | NP_001092090.1 | ||
| NM_001128911.1 | 2730 | Intron | NP_001122383.1 | ||
| NM_001128912.1 | 2730 | Intron | NP_001122384.1 | ||
| NM_001128913.1 | 2730 | Intron | NP_001122385.1 | ||
| NM_001128914.1 | 2730 | Intron | NP_001122386.1 | ||
| NM_005016.5 | 2730 | Intron | NP_005007.2 | ||
| NM_031989.4 | 2730 | Intron | NP_114366.1 |