HapMap
HapMap
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001281731.1 | 988 | Intron | NP_001268660.1 | ||
| NM_147190.3 | 988 | Intron | NP_671723.1 | ||
| XM_005269220.2 | 988 | Intron | XP_005269277.1 | ||
| XM_006719687.3 | 988 | Intron | XP_006719750.1 | ||
| XM_011538975.2 | 988 | Missense Mutation | CTC,TTC | L355F | XP_011537277.1 |
| XM_017020202.1 | 988 | Intron | XP_016875691.1 | ||
| XM_017020203.1 | 988 | Missense Mutation | CTC,TTC | L297F | XP_016875692.1 |
| XM_017020204.1 | 988 | Intron | XP_016875693.1 | ||
| XM_017020205.1 | 988 | Missense Mutation | CTC,TTC | L211F | XP_016875694.1 |