| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001278284.1 | 970 | Intron | NP_001265213.1 | ||
| NM_001278287.1 | 970 | Intron | NP_001265216.1 | ||
| NM_001278290.1 | 970 | Intron | NP_001265219.1 | ||
| NM_001278291.1 | 970 | Intron | NP_001265220.1 | ||
| NM_001278292.1 | 970 | Intron | NP_001265221.1 | ||
| NM_001318135.1 | 970 | Intron | NP_001305064.1 | ||
| NM_001318136.1 | 970 | Intron | NP_001305065.1 | ||
| NM_001318137.1 | 970 | UTR 3 | NP_001305066.1 | ||
| NM_017715.3 | 970 | UTR 3 | NP_060185.2 | ||
| NM_032924.4 | 970 | Intron | NP_116313.3 | ||
| XM_006716111.1 | 970 | Intron | XP_006716174.1 | ||
| XM_017012582.1 | 970 | Intron | XP_016868071.1 | ||
| XM_017012583.1 | 970 | Intron | XP_016868072.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_145914.2 | 970 | Missense Mutation | CGT,TGT | R276C | NP_666019.1 |
| XM_005250568.4 | 970 | Missense Mutation | CGT,TGT | R276C | XP_005250625.1 |
| XM_006716113.3 | 970 | Missense Mutation | CGT,TGT | R276C | XP_006716176.1 |
| XM_017012584.1 | 970 | Missense Mutation | CGT,TGT | R276C | XP_016868073.1 |
| XM_017012585.1 | 970 | Intron | XP_016868074.1 |