|
NM_002336.3:c.1003C>T
(LRP6)
MANE Select
|
NP_002327.2:p.Arg335Ter
|
|
ENST00000261349.9:c.1003C>T
(LRP6)
MANE Select
|
ENSP00000261349.4:p.Arg335Ter
|
|
NM_002336.2:c.1003C>T
(LRP6)
|
NP_002327.2:p.Arg335Ter
|
|
ENST00000261349.8:c.1003C>T
(LRP6)
|
ENSP00000261349.4:p.Arg335Ter
|
|
ENST00000298566.2:c.*25-5892G>A
(BCL2L14)
|
ENSP00000298566.1:n.*25-5892G>A
|
|
ENST00000538239.5:c.597C>T
(LRP6)
|
|
|
ENST00000543091.1:c.1003C>T
(LRP6)
|
ENSP00000442472.1:p.Arg335Ter
|
|
XM_006719078.2:c.1003C>T
(LRP6)
|
XP_006719141.1:p.Arg335Ter
|
|
XM_006719078.4:c.1003C>T
(LRP6)
|
XP_006719141.1:p.Arg335Ter
|
|
XM_011520671.1:c.550C>T
(LRP6)
|
XP_011518973.1:p.Arg184Ter
|
|
XM_011520671.3:c.550C>T
(LRP6)
|
XP_011518973.1:p.Arg184Ter
|
|
XR_002957325.1:n.1136C>T
(LRP6)
|
|
|
XR_429034.1:n.1136C>T
(LRP6)
|
|
|
XR_429035.1:n.1136C>T
(LRP6)
|
|
|
XR_429035.3:n.1136C>T
(LRP6)
|
|
