ENST00000261349.9:c.3801T>G
(LRP6)
MANE Select
|
ENSP00000261349.4:p.Ala1267=
|
|
ENST00000261349.8:c.3801T>G
(LRP6)
|
ENSP00000261349.4:p.Ala1267=
|
|
ENST00000298566.2:c.712-6846A>C
(BCL2L14)
|
ENSP00000298566.1:n.712-6846A>C
|
|
ENST00000538239.5:c.3395T>G
(LRP6)
|
|
|
ENST00000540415.1:n.122T>G
(LRP6)
|
|
|
ENST00000543091.1:c.3734-68T>G
(LRP6)
|
ENSP00000442472.1:n.3734-68T>G
|
|
NM_002336.2:c.3801T>G
(LRP6)
|
NP_002327.2:p.Ala1267=
|
|
XM_006719078.2:c.3801T>G
(LRP6)
|
XP_006719141.1:p.Ala1267=
|
|
XM_011520671.1:c.3348T>G
(LRP6)
|
XP_011518973.1:p.Ala1116=
|
|
XR_429034.1:n.3934T>G
(LRP6)
|
|
|
XR_429035.1:n.3934T>G
(LRP6)
|
|
|
XM_006719078.4:c.3801T>G
(LRP6)
|
XP_006719141.1:p.Ala1267=
|
|
XM_011520671.3:c.3348T>G
(LRP6)
|
XP_011518973.1:p.Ala1116=
|
|
XR_002957325.1:n.3934T>G
(LRP6)
|
|
|
XR_429035.3:n.3934T>G
(LRP6)
|
|
|
NM_002336.3:c.3801T>G
(LRP6)
MANE Select
|
NP_002327.2:p.Ala1267=
|
|