ENST00000342992.11:c.71132T>A
(TTN)
|
ENSP00000343764.6:p.Val23711Glu
|
|
ENST00000342175.11:c.52217T>A
(TTN)
|
ENSP00000340554.6:p.Val17406Glu
|
|
ENST00000359218.10:c.52016T>A
(TTN)
|
ENSP00000352154.5:p.Val17339Glu
|
|
ENST00000342175.10:c.52217T>A
(TTN)
|
ENSP00000340554.6:p.Val17406Glu
|
|
ENST00000342992.10:c.71132T>A
(TTN)
|
ENSP00000343764.6:p.Val23711Glu
|
|
ENST00000359218.9:c.52016T>A
(TTN)
|
ENSP00000352154.5:p.Val17339Glu
|
|
ENST00000460472.6:c.51641T>A
(TTN)
|
ENSP00000434586.1:p.Val17214Glu
|
|
ENST00000589042.5:c.78836T>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Val26279Glu
|
|
ENST00000591111.5:c.73913T>A
(TTN)
|
ENSP00000465570.1:p.Val24638Glu
|
|
ENST00000615779.4:c.73913T>A
(TTN)
|
ENSP00000483597.1:p.Val24638Glu
|
|
NM_001256850.1:c.73913T>A
(TTN)
|
NP_001243779.1:p.Val24638Glu
|
|
NM_001267550.2:c.78836T>A
(TTN)
MANE Select
|
NP_001254479.2:p.Val26279Glu
|
|
NM_003319.4:c.51641T>A
(TTN)
|
NP_003310.4:p.Val17214Glu
|
|
NM_133378.4:c.71132T>A
(TTN)
|
NP_596869.4:p.Val23711Glu
|
|
NM_133432.3:c.52016T>A
(TTN)
|
NP_597676.3:p.Val17339Glu
|
|
NM_133437.4:c.52217T>A
(TTN)
|
NP_597681.4:p.Val17406Glu
|
|
NR_038271.1:n.447-4004A>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-15276A>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.77933T>A
(TTN)
|
XP_011510031.1:p.Val25978Glu
|
|
XM_011511730.1:c.51827T>A
(TTN)
|
XP_011510032.1:p.Val17276Glu
|
|
XM_011511731.1:c.51686T>A
(TTN)
|
XP_011510033.1:p.Val17229Glu
|
|
XM_017004819.1:c.77729T>A
(TTN)
|
XP_016860308.1:p.Val25910Glu
|
|
XM_017004820.1:c.73127T>A
(TTN)
|
XP_016860309.1:p.Val24376Glu
|
|
XM_017004821.1:c.73124T>A
(TTN)
|
XP_016860310.1:p.Val24375Glu
|
|
XM_017004822.1:c.70166T>A
(TTN)
|
XP_016860311.1:p.Val23389Glu
|
|
XM_017004823.1:c.51782T>A
(TTN)
|
XP_016860312.1:p.Val17261Glu
|
|
XM_024453094.1:c.73277T>A
(TTN)
|
XP_024308862.1:p.Val24426Glu
|
|
XM_024453095.1:c.73274T>A
(TTN)
|
XP_024308863.1:p.Val24425Glu
|
|
XM_024453096.1:c.72707T>A
(TTN)
|
XP_024308864.1:p.Val24236Glu
|
|
XM_024453097.1:c.70049T>A
(TTN)
|
XP_024308865.1:p.Val23350Glu
|
|
XM_024453098.1:c.69968T>A
(TTN)
|
XP_024308866.1:p.Val23323Glu
|
|
XM_024453099.1:c.51731T>A
(TTN)
|
XP_024308867.1:p.Val17244Glu
|
|
XM_024453100.1:c.41585T>A
(TTN)
|
XP_024308868.1:p.Val13862Glu
|
|