ENST00000342992.11:c.88133T>G
(TTN)
|
ENSP00000343764.6:p.Leu29378Arg
|
|
ENST00000342175.11:c.69218T>G
(TTN)
|
ENSP00000340554.6:p.Leu23073Arg
|
|
ENST00000359218.10:c.69017T>G
(TTN)
|
ENSP00000352154.5:p.Leu23006Arg
|
|
ENST00000342175.10:c.69218T>G
(TTN)
|
ENSP00000340554.6:p.Leu23073Arg
|
|
ENST00000342992.10:c.88133T>G
(TTN)
|
ENSP00000343764.6:p.Leu29378Arg
|
|
ENST00000359218.9:c.69017T>G
(TTN)
|
ENSP00000352154.5:p.Leu23006Arg
|
|
ENST00000460472.6:c.68642T>G
(TTN)
|
ENSP00000434586.1:p.Leu22881Arg
|
|
ENST00000589042.5:c.95837T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu31946Arg
|
|
ENST00000591111.5:c.90914T>G
(TTN)
|
ENSP00000465570.1:p.Leu30305Arg
|
|
ENST00000615779.4:c.90914T>G
(TTN)
|
ENSP00000483597.1:p.Leu30305Arg
|
|
NM_001256850.1:c.90914T>G
(TTN)
|
NP_001243779.1:p.Leu30305Arg
|
|
NM_001267550.2:c.95837T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Leu31946Arg
|
|
NM_003319.4:c.68642T>G
(TTN)
|
NP_003310.4:p.Leu22881Arg
|
|
NM_133378.4:c.88133T>G
(TTN)
|
NP_596869.4:p.Leu29378Arg
|
|
NM_133432.3:c.69017T>G
(TTN)
|
NP_597676.3:p.Leu23006Arg
|
|
NM_133437.4:c.69218T>G
(TTN)
|
NP_597681.4:p.Leu23073Arg
|
|
NR_038271.1:n.446+20756A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+2031A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.94934T>G
(TTN)
|
XP_011510031.1:p.Leu31645Arg
|
|
XM_011511730.1:c.68828T>G
(TTN)
|
XP_011510032.1:p.Leu22943Arg
|
|
XM_011511731.1:c.68687T>G
(TTN)
|
XP_011510033.1:p.Leu22896Arg
|
|
XM_017004819.1:c.94730T>G
(TTN)
|
XP_016860308.1:p.Leu31577Arg
|
|
XM_017004820.1:c.90128T>G
(TTN)
|
XP_016860309.1:p.Leu30043Arg
|
|
XM_017004821.1:c.90125T>G
(TTN)
|
XP_016860310.1:p.Leu30042Arg
|
|
XM_017004822.1:c.87167T>G
(TTN)
|
XP_016860311.1:p.Leu29056Arg
|
|
XM_017004823.1:c.68783T>G
(TTN)
|
XP_016860312.1:p.Leu22928Arg
|
|
XM_024453094.1:c.90278T>G
(TTN)
|
XP_024308862.1:p.Leu30093Arg
|
|
XM_024453095.1:c.90275T>G
(TTN)
|
XP_024308863.1:p.Leu30092Arg
|
|
XM_024453096.1:c.89708T>G
(TTN)
|
XP_024308864.1:p.Leu29903Arg
|
|
XM_024453097.1:c.87050T>G
(TTN)
|
XP_024308865.1:p.Leu29017Arg
|
|
XM_024453098.1:c.86969T>G
(TTN)
|
XP_024308866.1:p.Leu28990Arg
|
|
XM_024453099.1:c.68732T>G
(TTN)
|
XP_024308867.1:p.Leu22911Arg
|
|
XM_024453100.1:c.58586T>G
(TTN)
|
XP_024308868.1:p.Leu19529Arg
|
|