ENST00000342992.11:c.51332C>A
(TTN)
|
ENSP00000343764.6:p.Ala17111Asp
|
|
ENST00000342175.11:c.32417C>A
(TTN)
|
ENSP00000340554.6:p.Ala10806Asp
|
|
ENST00000359218.10:c.32216C>A
(TTN)
|
ENSP00000352154.5:p.Ala10739Asp
|
|
ENST00000342175.10:c.32417C>A
(TTN)
|
ENSP00000340554.6:p.Ala10806Asp
|
|
ENST00000342992.10:c.51332C>A
(TTN)
|
ENSP00000343764.6:p.Ala17111Asp
|
|
ENST00000359218.9:c.32216C>A
(TTN)
|
ENSP00000352154.5:p.Ala10739Asp
|
|
ENST00000460472.6:c.31841C>A
(TTN)
|
ENSP00000434586.1:p.Ala10614Asp
|
|
ENST00000589042.5:c.59036C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ala19679Asp
|
|
ENST00000591111.5:c.54113C>A
(TTN)
|
ENSP00000465570.1:p.Ala18038Asp
|
|
ENST00000615779.4:c.54113C>A
(TTN)
|
ENSP00000483597.1:p.Ala18038Asp
|
|
NM_001256850.1:c.54113C>A
(TTN)
|
NP_001243779.1:p.Ala18038Asp
|
|
NM_001267550.2:c.59036C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Ala19679Asp
|
|
NM_003319.4:c.31841C>A
(TTN)
|
NP_003310.4:p.Ala10614Asp
|
|
NM_133378.4:c.51332C>A
(TTN)
|
NP_596869.4:p.Ala17111Asp
|
|
NM_133432.3:c.32216C>A
(TTN)
|
NP_597676.3:p.Ala10739Asp
|
|
NM_133437.4:c.32417C>A
(TTN)
|
NP_597681.4:p.Ala10806Asp
|
|
NR_038271.1:n.597-4513G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.3364+1769G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.58133C>A
(TTN)
|
XP_011510031.1:p.Ala19378Asp
|
|
XM_011511730.1:c.32027C>A
(TTN)
|
XP_011510032.1:p.Ala10676Asp
|
|
XM_011511731.1:c.31886C>A
(TTN)
|
XP_011510033.1:p.Ala10629Asp
|
|
XM_017004819.1:c.57929C>A
(TTN)
|
XP_016860308.1:p.Ala19310Asp
|
|
XM_017004820.1:c.53327C>A
(TTN)
|
XP_016860309.1:p.Ala17776Asp
|
|
XM_017004821.1:c.53324C>A
(TTN)
|
XP_016860310.1:p.Ala17775Asp
|
|
XM_017004822.1:c.50366C>A
(TTN)
|
XP_016860311.1:p.Ala16789Asp
|
|
XM_017004823.1:c.31982C>A
(TTN)
|
XP_016860312.1:p.Ala10661Asp
|
|
XM_024453094.1:c.53477C>A
(TTN)
|
XP_024308862.1:p.Ala17826Asp
|
|
XM_024453095.1:c.53474C>A
(TTN)
|
XP_024308863.1:p.Ala17825Asp
|
|
XM_024453096.1:c.52907C>A
(TTN)
|
XP_024308864.1:p.Ala17636Asp
|
|
XM_024453097.1:c.50249C>A
(TTN)
|
XP_024308865.1:p.Ala16750Asp
|
|
XM_024453098.1:c.50168C>A
(TTN)
|
XP_024308866.1:p.Ala16723Asp
|
|
XM_024453099.1:c.31931C>A
(TTN)
|
XP_024308867.1:p.Ala10644Asp
|
|
XM_024453100.1:c.21785C>A
(TTN)
|
XP_024308868.1:p.Ala7262Asp
|
|