ENST00000682565.1:c.11717T>A
|
ENSP00000507671.1:p.Val3906Glu
|
|
ENST00000682801.1:c.11167-765T>A
|
ENSP00000507862.1:n.11167-765T>A
|
|
ENST00000682859.1:c.11717T>A
|
ENSP00000508222.1:p.Val3906Glu
|
|
ENST00000683791.1:c.4803T>A
|
|
|
ENST00000684460.1:c.8998T>A
|
|
|
ENST00000684548.1:c.11717T>A
|
ENSP00000507421.1:p.Val3906Glu
|
|
ENST00000684590.1:c.6164T>A
|
ENSP00000507376.1:p.Val2055Glu
|
|
ENST00000684656.1:c.9182T>A
|
|
|
ENST00000613296.6:c.12098T>A
MANE Select
|
ENSP00000482968.1:p.Val4033Glu
|
|
ENST00000651057.1:c.2252T>A
|
ENSP00000498504.1:p.Val751Glu
|
|
ENST00000651434.1:c.3454T>A
|
|
|
ENST00000651750.1:c.1260+539T>A
|
|
|
ENST00000652487.1:c.3269T>A
|
|
|
ENST00000464408.3:n.273T>A
|
|
|
ENST00000484298.5:c.11972T>A
|
ENSP00000478155.1:p.Val3991Glu
|
|
ENST00000613296.4:c.12098T>A
|
ENSP00000482968.1:p.Val4033Glu
|
|
ENST00000620466.4:n.5901T>A
|
|
|
NM_015120.4:c.12101T>A , LRG_741t1:c.12101T>A
|
NP_055935.4:p.Val4034Glu
|
|
NM_001378454.1:c.12098T>A
MANE Select
|
NP_001365383.1:p.Val4033Glu
|
|