ENST00000342992.11:c.90392T>G
(TTN)
|
ENSP00000343764.6:p.Leu30131Arg
|
|
ENST00000342175.11:c.71477T>G
(TTN)
|
ENSP00000340554.6:p.Leu23826Arg
|
|
ENST00000359218.10:c.71276T>G
(TTN)
|
ENSP00000352154.5:p.Leu23759Arg
|
|
ENST00000342175.10:c.71477T>G
(TTN)
|
ENSP00000340554.6:p.Leu23826Arg
|
|
ENST00000342992.10:c.90392T>G
(TTN)
|
ENSP00000343764.6:p.Leu30131Arg
|
|
ENST00000359218.9:c.71276T>G
(TTN)
|
ENSP00000352154.5:p.Leu23759Arg
|
|
ENST00000460472.6:c.70901T>G
(TTN)
|
ENSP00000434586.1:p.Leu23634Arg
|
|
ENST00000589042.5:c.98096T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu32699Arg
|
|
ENST00000591111.5:c.93173T>G
(TTN)
|
ENSP00000465570.1:p.Leu31058Arg
|
|
ENST00000615779.4:c.93173T>G
(TTN)
|
ENSP00000483597.1:p.Leu31058Arg
|
|
NM_001256850.1:c.93173T>G
(TTN)
|
NP_001243779.1:p.Leu31058Arg
|
|
NM_001267550.2:c.98096T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Leu32699Arg
|
|
NM_003319.4:c.70901T>G
(TTN)
|
NP_003310.4:p.Leu23634Arg
|
|
NM_133378.4:c.90392T>G
(TTN)
|
NP_596869.4:p.Leu30131Arg
|
|
NM_133432.3:c.71276T>G
(TTN)
|
NP_597676.3:p.Leu23759Arg
|
|
NM_133437.4:c.71477T>G
(TTN)
|
NP_597681.4:p.Leu23826Arg
|
|
NR_038271.1:n.446+16434A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.1841-37A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.97193T>G
(TTN)
|
XP_011510031.1:p.Leu32398Arg
|
|
XM_011511730.1:c.71087T>G
(TTN)
|
XP_011510032.1:p.Leu23696Arg
|
|
XM_011511731.1:c.70946T>G
(TTN)
|
XP_011510033.1:p.Leu23649Arg
|
|
XM_017004819.1:c.96989T>G
(TTN)
|
XP_016860308.1:p.Leu32330Arg
|
|
XM_017004820.1:c.92387T>G
(TTN)
|
XP_016860309.1:p.Leu30796Arg
|
|
XM_017004821.1:c.92384T>G
(TTN)
|
XP_016860310.1:p.Leu30795Arg
|
|
XM_017004822.1:c.89426T>G
(TTN)
|
XP_016860311.1:p.Leu29809Arg
|
|
XM_017004823.1:c.71042T>G
(TTN)
|
XP_016860312.1:p.Leu23681Arg
|
|
XM_024453094.1:c.92537T>G
(TTN)
|
XP_024308862.1:p.Leu30846Arg
|
|
XM_024453095.1:c.92534T>G
(TTN)
|
XP_024308863.1:p.Leu30845Arg
|
|
XM_024453096.1:c.91967T>G
(TTN)
|
XP_024308864.1:p.Leu30656Arg
|
|
XM_024453097.1:c.89309T>G
(TTN)
|
XP_024308865.1:p.Leu29770Arg
|
|
XM_024453098.1:c.89228T>G
(TTN)
|
XP_024308866.1:p.Leu29743Arg
|
|
XM_024453099.1:c.70991T>G
(TTN)
|
XP_024308867.1:p.Leu23664Arg
|
|
XM_024453100.1:c.60845T>G
(TTN)
|
XP_024308868.1:p.Leu20282Arg
|
|