| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001320046.1 | 2000 | Intron | NP_001306975.1 | ||
| NM_032630.2 | 2000 | Intron | NP_116019.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001267827.1 | 2000 | Missense Mutation | CCT,CTT | P596L | NP_001254756.1 |
| NM_001267828.1 | 2000 | Missense Mutation | CCT,CTT | P596L | NP_001254757.1 |
| NM_018335.4 | 2000 | Missense Mutation | CCT,CTT | P712L | NP_060805.3 |
| XM_006720203.3 | 2000 | Missense Mutation | CCT,CTT | P624L | XP_006720266.2 |
| XM_011536945.1 | 2000 | Missense Mutation | CCT,CTT | P746L | XP_011535247.1 |
| XM_011536946.2 | 2000 | Missense Mutation | CCT,CTT | P696L | XP_011535248.1 |
| XM_011536948.2 | 2000 | Missense Mutation | CCT,CTT | P596L | XP_011535250.1 |
| XM_011536949.2 | 2000 | Intron | XP_011535251.1 | ||
| XM_011536950.2 | 2000 | Intron | XP_011535252.1 | ||
| XM_017021447.1 | 2000 | Missense Mutation | CCT,CTT | P662L | XP_016876936.1 |
| XM_017021448.1 | 2000 | Intron | XP_016876937.1 | ||
| XM_017021449.1 | 2000 | Missense Mutation | CCT,CTT | P377L | XP_016876938.1 |
| XM_017021450.1 | 2000 | Intron | XP_016876939.1 | ||
| XM_017021451.1 | 2000 | Intron | XP_016876940.1 |