ENST00000342992.11:c.87930T>C
(TTN)
|
ENSP00000343764.6:p.Asp29310=
|
|
ENST00000342175.11:c.69015T>C
(TTN)
|
ENSP00000340554.6:p.Asp23005=
|
|
ENST00000359218.10:c.68814T>C
(TTN)
|
ENSP00000352154.5:p.Asp22938=
|
|
ENST00000342175.10:c.69015T>C
(TTN)
|
ENSP00000340554.6:p.Asp23005=
|
|
ENST00000342992.10:c.87930T>C
(TTN)
|
ENSP00000343764.6:p.Asp29310=
|
|
ENST00000359218.9:c.68814T>C
(TTN)
|
ENSP00000352154.5:p.Asp22938=
|
|
ENST00000460472.6:c.68439T>C
(TTN)
|
ENSP00000434586.1:p.Asp22813=
|
|
ENST00000589042.5:c.95634T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp31878=
|
|
ENST00000591111.5:c.90711T>C
(TTN)
|
ENSP00000465570.1:p.Asp30237=
|
|
ENST00000615779.4:c.90711T>C
(TTN)
|
ENSP00000483597.1:p.Asp30237=
|
|
NM_001256850.1:c.90711T>C
(TTN)
|
NP_001243779.1:p.Asp30237=
|
|
NM_001267550.2:c.95634T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Asp31878=
|
|
NM_003319.4:c.68439T>C
(TTN)
|
NP_003310.4:p.Asp22813=
|
|
NM_133378.4:c.87930T>C
(TTN)
|
NP_596869.4:p.Asp29310=
|
|
NM_133432.3:c.68814T>C
(TTN)
|
NP_597676.3:p.Asp22938=
|
|
NM_133437.4:c.69015T>C
(TTN)
|
NP_597681.4:p.Asp23005=
|
|
NR_038271.1:n.446+21840A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+3115A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.94731T>C
(TTN)
|
XP_011510031.1:p.Asp31577=
|
|
XM_011511730.1:c.68625T>C
(TTN)
|
XP_011510032.1:p.Asp22875=
|
|
XM_011511731.1:c.68484T>C
(TTN)
|
XP_011510033.1:p.Asp22828=
|
|
XM_017004819.1:c.94527T>C
(TTN)
|
XP_016860308.1:p.Asp31509=
|
|
XM_017004820.1:c.89925T>C
(TTN)
|
XP_016860309.1:p.Asp29975=
|
|
XM_017004821.1:c.89922T>C
(TTN)
|
XP_016860310.1:p.Asp29974=
|
|
XM_017004822.1:c.86964T>C
(TTN)
|
XP_016860311.1:p.Asp28988=
|
|
XM_017004823.1:c.68580T>C
(TTN)
|
XP_016860312.1:p.Asp22860=
|
|
XM_024453094.1:c.90075T>C
(TTN)
|
XP_024308862.1:p.Asp30025=
|
|
XM_024453095.1:c.90072T>C
(TTN)
|
XP_024308863.1:p.Asp30024=
|
|
XM_024453096.1:c.89505T>C
(TTN)
|
XP_024308864.1:p.Asp29835=
|
|
XM_024453097.1:c.86847T>C
(TTN)
|
XP_024308865.1:p.Asp28949=
|
|
XM_024453098.1:c.86766T>C
(TTN)
|
XP_024308866.1:p.Asp28922=
|
|
XM_024453099.1:c.68529T>C
(TTN)
|
XP_024308867.1:p.Asp22843=
|
|
XM_024453100.1:c.58383T>C
(TTN)
|
XP_024308868.1:p.Asp19461=
|
|