ENST00000342992.11:c.84170G>A
(TTN)
|
ENSP00000343764.6:p.Gly28057Glu
|
|
ENST00000342175.11:c.65255G>A
(TTN)
|
ENSP00000340554.6:p.Gly21752Glu
|
|
ENST00000359218.10:c.65054G>A
(TTN)
|
ENSP00000352154.5:p.Gly21685Glu
|
|
ENST00000342175.10:c.65255G>A
(TTN)
|
ENSP00000340554.6:p.Gly21752Glu
|
|
ENST00000342992.10:c.84170G>A
(TTN)
|
ENSP00000343764.6:p.Gly28057Glu
|
|
ENST00000359218.9:c.65054G>A
(TTN)
|
ENSP00000352154.5:p.Gly21685Glu
|
|
ENST00000460472.6:c.64679G>A
(TTN)
|
ENSP00000434586.1:p.Gly21560Glu
|
|
ENST00000589042.5:c.91874G>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gly30625Glu
|
|
ENST00000591111.5:c.86951G>A
(TTN)
|
ENSP00000465570.1:p.Gly28984Glu
|
|
ENST00000615779.4:c.86951G>A
(TTN)
|
ENSP00000483597.1:p.Gly28984Glu
|
|
NM_001256850.1:c.86951G>A
(TTN)
|
NP_001243779.1:p.Gly28984Glu
|
|
NM_001267550.2:c.91874G>A
(TTN)
MANE Select
|
NP_001254479.2:p.Gly30625Glu
|
|
NM_003319.4:c.64679G>A
(TTN)
|
NP_003310.4:p.Gly21560Glu
|
|
NM_133378.4:c.84170G>A
(TTN)
|
NP_596869.4:p.Gly28057Glu
|
|
NM_133432.3:c.65054G>A
(TTN)
|
NP_597676.3:p.Gly21685Glu
|
|
NM_133437.4:c.65255G>A
(TTN)
|
NP_597681.4:p.Gly21752Glu
|
|
NR_038271.1:n.447-21452C>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+7487C>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.90971G>A
(TTN)
|
XP_011510031.1:p.Gly30324Glu
|
|
XM_011511730.1:c.64865G>A
(TTN)
|
XP_011510032.1:p.Gly21622Glu
|
|
XM_011511731.1:c.64724G>A
(TTN)
|
XP_011510033.1:p.Gly21575Glu
|
|
XM_017004819.1:c.90767G>A
(TTN)
|
XP_016860308.1:p.Gly30256Glu
|
|
XM_017004820.1:c.86165G>A
(TTN)
|
XP_016860309.1:p.Gly28722Glu
|
|
XM_017004821.1:c.86162G>A
(TTN)
|
XP_016860310.1:p.Gly28721Glu
|
|
XM_017004822.1:c.83204G>A
(TTN)
|
XP_016860311.1:p.Gly27735Glu
|
|
XM_017004823.1:c.64820G>A
(TTN)
|
XP_016860312.1:p.Gly21607Glu
|
|
XM_024453094.1:c.86315G>A
(TTN)
|
XP_024308862.1:p.Gly28772Glu
|
|
XM_024453095.1:c.86312G>A
(TTN)
|
XP_024308863.1:p.Gly28771Glu
|
|
XM_024453096.1:c.85745G>A
(TTN)
|
XP_024308864.1:p.Gly28582Glu
|
|
XM_024453097.1:c.83087G>A
(TTN)
|
XP_024308865.1:p.Gly27696Glu
|
|
XM_024453098.1:c.83006G>A
(TTN)
|
XP_024308866.1:p.Gly27669Glu
|
|
XM_024453099.1:c.64769G>A
(TTN)
|
XP_024308867.1:p.Gly21590Glu
|
|
XM_024453100.1:c.54623G>A
(TTN)
|
XP_024308868.1:p.Gly18208Glu
|
|