ENST00000261349.9:c.3895C>A
(LRP6)
MANE Select
|
ENSP00000261349.4:p.Gln1299Lys
|
|
ENST00000261349.8:c.3895C>A
(LRP6)
|
ENSP00000261349.4:p.Gln1299Lys
|
|
ENST00000298566.2:c.712-6940G>T
(BCL2L14)
|
ENSP00000298566.1:n.712-6940G>T
|
|
ENST00000538239.5:c.3489C>A
(LRP6)
|
|
|
ENST00000540415.1:n.216C>A
(LRP6)
|
|
|
ENST00000543091.1:c.3760C>A
(LRP6)
|
ENSP00000442472.1:p.Gln1254Lys
|
|
NM_002336.2:c.3895C>A
(LRP6)
|
NP_002327.2:p.Gln1299Lys
|
|
XM_006719078.2:c.3895C>A
(LRP6)
|
XP_006719141.1:p.Gln1299Lys
|
|
XM_011520671.1:c.3442C>A
(LRP6)
|
XP_011518973.1:p.Gln1148Lys
|
|
XR_429034.1:n.4028C>A
(LRP6)
|
|
|
XR_429035.1:n.4028C>A
(LRP6)
|
|
|
XM_006719078.4:c.3895C>A
(LRP6)
|
XP_006719141.1:p.Gln1299Lys
|
|
XM_011520671.3:c.3442C>A
(LRP6)
|
XP_011518973.1:p.Gln1148Lys
|
|
XR_002957325.1:n.4028C>A
(LRP6)
|
|
|
XR_429035.3:n.4028C>A
(LRP6)
|
|
|
NM_002336.3:c.3895C>A
(LRP6)
MANE Select
|
NP_002327.2:p.Gln1299Lys
|
|