HapMap
HapMap
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_199350.3 | 972 | Missense Mutation | AAG,AGG | K415R | NP_955382.3 |
| XM_011518655.1 | 972 | Missense Mutation | AAG,AGG | K415R | XP_011516957.1 |
| XM_011518656.1 | 972 | Missense Mutation | AAG,AGG | K415R | XP_011516958.1 |
| XM_011518657.2 | 972 | Missense Mutation | AAG,AGG | K320R | XP_011516959.1 |
| XM_011518658.2 | 972 | Missense Mutation | AAG,AGG | K319R | XP_011516960.1 |
| XM_011518659.1 | 972 | Intron | XP_011516961.1 | ||
| XM_011518660.1 | 972 | Intron | XP_011516962.1 | ||
| XM_011518661.2 | 972 | Missense Mutation | AAG,AGG | K231R | XP_011516963.1 |
| XM_011518662.2 | 972 | Missense Mutation | AAG,AGG | K230R | XP_011516964.1 |
| XM_011518663.1 | 972 | Intron | XP_011516965.1 | ||
| XM_017014708.1 | 972 | Intron | XP_016870197.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001286796.1 | 972 | Intron | NP_001273725.1 | ||
| NM_001286797.1 | 972 | Intron | NP_001273726.1 | ||
| NM_001286798.1 | 972 | Intron | NP_001273727.1 | ||
| NM_001286799.1 | 972 | Intron | NP_001273728.1 | ||
| NM_001286800.1 | 972 | Intron | NP_001273729.1 | ||
| NM_001286801.1 | 972 | Intron | NP_001273730.1 | ||
| NM_001286802.1 | 972 | Intron | NP_001273731.1 | ||
| NM_001286803.1 | 972 | Intron | NP_001273732.1 | ||
| NM_014064.3 | 972 | Intron | NP_054783.2 | ||
| XM_005251939.3 | 972 | Intron | XP_005251996.1 | ||
| XM_017014642.1 | 972 | Intron | XP_016870131.1 |