|
ENST00000700088.1:c.1397-313G>A
(MASP2)
|
ENSP00000514787.1:n.1397-313G>A
|
|
|
ENST00000240185.8:c.1097C>T
(TARDBP)
MANE Select
|
ENSP00000240185.4:p.Ala366Val
|
|
|
ENST00000639083.1:c.1097C>T
(TARDBP)
|
ENSP00000491203.1:p.Ala366Val
|
|
|
ENST00000639599.1:c.832+265C>T
(TARDBP)
|
ENSP00000492196.1:n.832+265C>T
|
|
|
ENST00000649624.1:c.768+329C>T
(TARDBP)
|
ENSP00000497327.1:n.768+329C>T
|
|
|
ENST00000240185.7:c.1097C>T
(TARDBP)
|
ENSP00000240185.3:p.Ala366Val
|
|
|
ENST00000315091.7:c.832+265C>T
(TARDBP)
|
ENSP00000313129.3:n.832+265C>T
|
|
|
ENST00000439080.6:c.*678C>T
(TARDBP)
|
ENSP00000404666.3:n.*678C>T
|
|
|
ENST00000473869.5:c.841+256C>T
(TARDBP)
|
ENSP00000432132.1:n.841+256C>T
|
|
|
ENST00000477447.6:c.140+256C>T
(TARDBP)
|
|
|
|
ENST00000610369.4:c.319+256C>T
(TARDBP)
|
ENSP00000482559.1:n.319+256C>T
|
|
|
ENST00000611136.4:c.212+265C>T
|
|
|
|
ENST00000611963.4:c.472+265C>T
(TARDBP)
|
ENSP00000481330.1:n.472+265C>T
|
|
|
ENST00000612542.1:c.107+256C>T
|
|
|
|
ENST00000614494.1:c.221+329C>T
(TARDBP)
|
|
|
|
ENST00000614757.4:c.841+256C>T
|
ENSP00000481867.1:n.841+256C>T
|
|
|
ENST00000616545.4:c.841+256C>T
(TARDBP)
|
ENSP00000484722.1:n.841+256C>T
|
|
|
ENST00000617172.4:c.582+256C>T
(TARDBP)
|
|
|
|
ENST00000619555.4:c.392+256C>T
(TARDBP)
|
|
|
|
ENST00000620505.1:c.199C>T
(TARDBP)
|
|
|
|
ENST00000620632.4:c.392+256C>T
(TARDBP)
|
|
|
|
ENST00000621790.4:c.859+238C>T
(TARDBP)
|
ENSP00000482191.1:n.859+238C>T
|
|
|
ENST00000622057.4:c.579+265C>T
(TARDBP)
|
|
|
|
ENST00000629725.2:c.841+256C>T
(TARDBP)
|
ENSP00000486989.1:n.841+256C>T
|
|
|
NM_007375.3:c.1097C>T , LRG_659t1:c.1097C>T
(TARDBP)
|
NP_031401.1:p.Ala366Val
|
|
|
XR_946596.1:n.1219C>T
(TARDBP)
|
|
|
|
XR_946597.1:n.1219C>T
(TARDBP)
|
|
|
|
XM_017000863.2:c.1097C>T
(TARDBP)
|
XP_016856352.1:p.Ala366Val
|
|
|
XM_017000864.2:c.1097C>T
(TARDBP)
|
XP_016856353.1:p.Ala366Val
|
|
|
XM_017000865.2:c.1097C>T
(TARDBP)
|
XP_016856354.1:p.Ala366Val
|
|
|
XM_017000866.2:c.1097C>T
(TARDBP)
|
XP_016856355.1:p.Ala366Val
|
|
|
XM_017000867.2:c.1097C>T
(TARDBP)
|
XP_016856356.1:p.Ala366Val
|
|
|
XM_017000868.2:c.1097C>T
(TARDBP)
|
XP_016856357.1:p.Ala366Val
|
|
|
NM_007375.4:c.1097C>T
(TARDBP)
MANE Select
|
NP_031401.1:p.Ala366Val
|
|
