ENST00000342992.11:c.86278C>A
(TTN)
|
ENSP00000343764.6:p.Leu28760Met
|
|
ENST00000342175.11:c.67363C>A
(TTN)
|
ENSP00000340554.6:p.Leu22455Met
|
|
ENST00000359218.10:c.67162C>A
(TTN)
|
ENSP00000352154.5:p.Leu22388Met
|
|
ENST00000342175.10:c.67363C>A
(TTN)
|
ENSP00000340554.6:p.Leu22455Met
|
|
ENST00000342992.10:c.86278C>A
(TTN)
|
ENSP00000343764.6:p.Leu28760Met
|
|
ENST00000359218.9:c.67162C>A
(TTN)
|
ENSP00000352154.5:p.Leu22388Met
|
|
ENST00000460472.6:c.66787C>A
(TTN)
|
ENSP00000434586.1:p.Leu22263Met
|
|
ENST00000589042.5:c.93982C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu31328Met
|
|
ENST00000591111.5:c.89059C>A
(TTN)
|
ENSP00000465570.1:p.Leu29687Met
|
|
ENST00000615779.4:c.89059C>A
(TTN)
|
ENSP00000483597.1:p.Leu29687Met
|
|
NM_001256850.1:c.89059C>A
(TTN)
|
NP_001243779.1:p.Leu29687Met
|
|
NM_001267550.2:c.93982C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Leu31328Met
|
|
NM_003319.4:c.66787C>A
(TTN)
|
NP_003310.4:p.Leu22263Met
|
|
NM_133378.4:c.86278C>A
(TTN)
|
NP_596869.4:p.Leu28760Met
|
|
NM_133432.3:c.67162C>A
(TTN)
|
NP_597676.3:p.Leu22388Met
|
|
NM_133437.4:c.67363C>A
(TTN)
|
NP_597681.4:p.Leu22455Met
|
|
NR_038271.1:n.447-23656G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+5283G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.93079C>A
(TTN)
|
XP_011510031.1:p.Leu31027Met
|
|
XM_011511730.1:c.66973C>A
(TTN)
|
XP_011510032.1:p.Leu22325Met
|
|
XM_011511731.1:c.66832C>A
(TTN)
|
XP_011510033.1:p.Leu22278Met
|
|
XM_017004819.1:c.92875C>A
(TTN)
|
XP_016860308.1:p.Leu30959Met
|
|
XM_017004820.1:c.88273C>A
(TTN)
|
XP_016860309.1:p.Leu29425Met
|
|
XM_017004821.1:c.88270C>A
(TTN)
|
XP_016860310.1:p.Leu29424Met
|
|
XM_017004822.1:c.85312C>A
(TTN)
|
XP_016860311.1:p.Leu28438Met
|
|
XM_017004823.1:c.66928C>A
(TTN)
|
XP_016860312.1:p.Leu22310Met
|
|
XM_024453094.1:c.88423C>A
(TTN)
|
XP_024308862.1:p.Leu29475Met
|
|
XM_024453095.1:c.88420C>A
(TTN)
|
XP_024308863.1:p.Leu29474Met
|
|
XM_024453096.1:c.87853C>A
(TTN)
|
XP_024308864.1:p.Leu29285Met
|
|
XM_024453097.1:c.85195C>A
(TTN)
|
XP_024308865.1:p.Leu28399Met
|
|
XM_024453098.1:c.85114C>A
(TTN)
|
XP_024308866.1:p.Leu28372Met
|
|
XM_024453099.1:c.66877C>A
(TTN)
|
XP_024308867.1:p.Leu22293Met
|
|
XM_024453100.1:c.56731C>A
(TTN)
|
XP_024308868.1:p.Leu18911Met
|
|