ENST00000322344.8:c.993G>A
MANE Select
|
ENSP00000323511.2:p.Trp331Ter
|
|
ENST00000322344.7:c.993G>A
|
ENSP00000323511.2:p.Trp331Ter
|
|
ENST00000593706.3:n.348G>A
|
|
|
ENST00000593946.5:c.*920G>A
|
ENSP00000468896.1:n.*920G>A
|
|
ENST00000594661.5:n.1494G>A
|
|
|
ENST00000596014.5:c.993G>A
|
ENSP00000472300.1:p.Trp331Ter
|
|
ENST00000600573.5:c.937-126G>A
|
ENSP00000469826.1:n.937-126G>A
|
|
ENST00000600910.5:c.993G>A
|
ENSP00000473137.1:p.Trp331Ter
|
|
ENST00000625216.2:c.171G>A
|
ENSP00000486898.1:p.Trp57Ter
|
|
ENST00000627232.2:c.913G>A
|
ENSP00000486037.1:n.913G>A
|
|
ENST00000627317.1:c.614G>A
|
|
|
ENST00000629179.1:n.764G>A
|
|
|
ENST00000631020.2:c.885G>A
|
ENSP00000486707.1:p.Trp295Ter
|
|
NM_007254.3:c.993G>A
|
NP_009185.2:p.Trp331Ter
|
|
NM_007254.4:c.993G>A
MANE Select
|
NP_009185.2:p.Trp331Ter
|
|