ENST00000342992.11:c.51331G>A
(TTN)
|
ENSP00000343764.6:p.Ala17111Thr
|
|
ENST00000342175.11:c.32416G>A
(TTN)
|
ENSP00000340554.6:p.Ala10806Thr
|
|
ENST00000359218.10:c.32215G>A
(TTN)
|
ENSP00000352154.5:p.Ala10739Thr
|
|
ENST00000342175.10:c.32416G>A
(TTN)
|
ENSP00000340554.6:p.Ala10806Thr
|
|
ENST00000342992.10:c.51331G>A
(TTN)
|
ENSP00000343764.6:p.Ala17111Thr
|
|
ENST00000359218.9:c.32215G>A
(TTN)
|
ENSP00000352154.5:p.Ala10739Thr
|
|
ENST00000460472.6:c.31840G>A
(TTN)
|
ENSP00000434586.1:p.Ala10614Thr
|
|
ENST00000589042.5:c.59035G>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ala19679Thr
|
|
ENST00000591111.5:c.54112G>A
(TTN)
|
ENSP00000465570.1:p.Ala18038Thr
|
|
ENST00000615779.4:c.54112G>A
(TTN)
|
ENSP00000483597.1:p.Ala18038Thr
|
|
NM_001256850.1:c.54112G>A
(TTN)
|
NP_001243779.1:p.Ala18038Thr
|
|
NM_001267550.2:c.59035G>A
(TTN)
MANE Select
|
NP_001254479.2:p.Ala19679Thr
|
|
NM_003319.4:c.31840G>A
(TTN)
|
NP_003310.4:p.Ala10614Thr
|
|
NM_133378.4:c.51331G>A
(TTN)
|
NP_596869.4:p.Ala17111Thr
|
|
NM_133432.3:c.32215G>A
(TTN)
|
NP_597676.3:p.Ala10739Thr
|
|
NM_133437.4:c.32416G>A
(TTN)
|
NP_597681.4:p.Ala10806Thr
|
|
NR_038271.1:n.597-4423C>T
(TTN-AS1)
|
|
|
NR_038272.1:n.3364+1859C>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.58132G>A
(TTN)
|
XP_011510031.1:p.Ala19378Thr
|
|
XM_011511730.1:c.32026G>A
(TTN)
|
XP_011510032.1:p.Ala10676Thr
|
|
XM_011511731.1:c.31885G>A
(TTN)
|
XP_011510033.1:p.Ala10629Thr
|
|
XM_017004819.1:c.57928G>A
(TTN)
|
XP_016860308.1:p.Ala19310Thr
|
|
XM_017004820.1:c.53326G>A
(TTN)
|
XP_016860309.1:p.Ala17776Thr
|
|
XM_017004821.1:c.53323G>A
(TTN)
|
XP_016860310.1:p.Ala17775Thr
|
|
XM_017004822.1:c.50365G>A
(TTN)
|
XP_016860311.1:p.Ala16789Thr
|
|
XM_017004823.1:c.31981G>A
(TTN)
|
XP_016860312.1:p.Ala10661Thr
|
|
XM_024453094.1:c.53476G>A
(TTN)
|
XP_024308862.1:p.Ala17826Thr
|
|
XM_024453095.1:c.53473G>A
(TTN)
|
XP_024308863.1:p.Ala17825Thr
|
|
XM_024453096.1:c.52906G>A
(TTN)
|
XP_024308864.1:p.Ala17636Thr
|
|
XM_024453097.1:c.50248G>A
(TTN)
|
XP_024308865.1:p.Ala16750Thr
|
|
XM_024453098.1:c.50167G>A
(TTN)
|
XP_024308866.1:p.Ala16723Thr
|
|
XM_024453099.1:c.31930G>A
(TTN)
|
XP_024308867.1:p.Ala10644Thr
|
|
XM_024453100.1:c.21784G>A
(TTN)
|
XP_024308868.1:p.Ala7262Thr
|
|