ENST00000322344.8:c.1433T>A
MANE Select
|
ENSP00000323511.2:p.Val478Asp
|
|
ENST00000636840.1:c.59+144T>A
|
|
|
ENST00000640501.1:c.39T>A
|
|
|
ENST00000322344.7:c.1433T>A
|
ENSP00000323511.2:p.Val478Asp
|
|
ENST00000593946.5:c.*1360T>A
|
ENSP00000468896.1:n.*1360T>A
|
|
ENST00000594661.5:n.1934T>A
|
|
|
ENST00000595081.5:n.336T>A
|
|
|
ENST00000596014.5:c.1433T>A
|
ENSP00000472300.1:p.Val478Asp
|
|
ENST00000597965.2:c.140T>A
|
ENSP00000471097.2:p.Val47Asp
|
|
ENST00000599454.5:n.353T>A
|
|
|
ENST00000600573.5:c.1340T>A
|
ENSP00000469826.1:p.Val447Asp
|
|
ENST00000600910.5:c.1323T>A
|
ENSP00000473137.1:p.Gly441=
|
|
ENST00000601816.3:n.505T>A
|
|
|
ENST00000625216.2:c.514T>A
|
ENSP00000486898.1:n.514T>A
|
|
ENST00000627232.2:c.1353T>A
|
ENSP00000486037.1:n.1353T>A
|
|
ENST00000631020.2:c.1325T>A
|
ENSP00000486707.1:p.Val442Asp
|
|
NM_007254.3:c.1433T>A
|
NP_009185.2:p.Val478Asp
|
|
NM_007254.4:c.1433T>A
MANE Select
|
NP_009185.2:p.Val478Asp
|
|