Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001040715.1 | 855 | Intron | NP_001035805.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001185057.2 | 855 | Missense Mutation | GCT,GGT | A218G | NP_001171986.1 |
NM_001276307.1 | 855 | UTR 3 | NP_001263236.1 | ||
NM_001276309.1 | 855 | UTR 3 | NP_001263238.1 | ||
NM_001276311.1 | 855 | Missense Mutation | GCT,GGT | A180G | NP_001263240.1 |
NM_001276312.1 | 855 | UTR 3 | NP_001263241.1 | ||
NM_001276319.1 | 855 | UTR 3 | NP_001263248.1 | ||
NM_003946.6 | 855 | UTR 3 | NP_003937.1 | ||
XM_005256217.2 | 855 | Missense Mutation | GCT,GGT | A280G | XP_005256274.1 |
XM_005256219.3 | 855 | Missense Mutation | GCT,GGT | A242G | XP_005256276.1 |
XM_011523424.2 | 855 | Missense Mutation | CTG,GTG | L219V | XP_011521726.1 |
XM_017023843.1 | 855 | UTR 3 | XP_016879332.1 |