Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001289082.1 | 926 | UTR 3 | NP_001276011.1 | ||
NM_001289083.1 | 926 | UTR 3 | NP_001276012.1 | ||
NM_001289084.1 | 926 | Missense Mutation | ACG,ATG | T254M | NP_001276013.1 |
NM_001289085.1 | 926 | Missense Mutation | ACG,ATG | T242M | NP_001276014.1 |
NM_001289086.1 | 926 | UTR 3 | NP_001276015.1 | ||
NM_001289087.1 | 926 | UTR 3 | NP_001276016.1 | ||
NM_139018.4 | 926 | Missense Mutation | ACG,ATG | T239M | NP_620587.2 |
XM_017024212.1 | 926 | Missense Mutation | ACG,ATG | T258M | XP_016879701.1 |
XM_017024213.1 | 926 | UTR 3 | XP_016879702.1 | ||
XM_017024214.1 | 926 | UTR 3 | XP_016879703.1 | ||
XM_017024215.1 | 926 | UTR 3 | XP_016879704.1 | ||
XM_017024216.1 | 926 | UTR 3 | XP_016879705.1 | ||
XM_017024217.1 | 926 | UTR 3 | XP_016879706.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001006638.2 | 926 | Intron | NP_001006639.1 | ||
NM_001163989.1 | 926 | Intron | NP_001157461.1 | ||
NM_001163990.1 | 926 | Intron | NP_001157462.1 | ||
NM_175738.4 | 926 | Intron | NP_783865.1 | ||
XM_005257288.4 | 926 | Intron | XP_005257345.1 |