ENST00000342992.11:c.60804T>A
(TTN)
|
ENSP00000343764.6:p.Val20268=
|
|
ENST00000342175.11:c.41889T>A
(TTN)
|
ENSP00000340554.6:p.Val13963=
|
|
ENST00000359218.10:c.41688T>A
(TTN)
|
ENSP00000352154.5:p.Val13896=
|
|
ENST00000342175.10:c.41889T>A
(TTN)
|
ENSP00000340554.6:p.Val13963=
|
|
ENST00000342992.10:c.60804T>A
(TTN)
|
ENSP00000343764.6:p.Val20268=
|
|
ENST00000359218.9:c.41688T>A
(TTN)
|
ENSP00000352154.5:p.Val13896=
|
|
ENST00000460472.6:c.41313T>A
(TTN)
|
ENSP00000434586.1:p.Val13771=
|
|
ENST00000589042.5:c.68508T>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Val22836=
|
|
ENST00000591111.5:c.63585T>A
(TTN)
|
ENSP00000465570.1:p.Val21195=
|
|
ENST00000615779.4:c.63585T>A
(TTN)
|
ENSP00000483597.1:p.Val21195=
|
|
NM_001256850.1:c.63585T>A
(TTN)
|
NP_001243779.1:p.Val21195=
|
|
NM_001267550.2:c.68508T>A
(TTN)
MANE Select
|
NP_001254479.2:p.Val22836=
|
|
NM_003319.4:c.41313T>A
(TTN)
|
NP_003310.4:p.Val13771=
|
|
NM_133378.4:c.60804T>A
(TTN)
|
NP_596869.4:p.Val20268=
|
|
NM_133432.3:c.41688T>A
(TTN)
|
NP_597676.3:p.Val13896=
|
|
NM_133437.4:c.41889T>A
(TTN)
|
NP_597681.4:p.Val13963=
|
|
NR_038271.1:n.596+6558A>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-4565A>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.67605T>A
(TTN)
|
XP_011510031.1:p.Val22535=
|
|
XM_011511730.1:c.41499T>A
(TTN)
|
XP_011510032.1:p.Val13833=
|
|
XM_011511731.1:c.41358T>A
(TTN)
|
XP_011510033.1:p.Val13786=
|
|
XM_017004819.1:c.67401T>A
(TTN)
|
XP_016860308.1:p.Val22467=
|
|
XM_017004820.1:c.62799T>A
(TTN)
|
XP_016860309.1:p.Val20933=
|
|
XM_017004821.1:c.62796T>A
(TTN)
|
XP_016860310.1:p.Val20932=
|
|
XM_017004822.1:c.59838T>A
(TTN)
|
XP_016860311.1:p.Val19946=
|
|
XM_017004823.1:c.41454T>A
(TTN)
|
XP_016860312.1:p.Val13818=
|
|
XM_024453094.1:c.62949T>A
(TTN)
|
XP_024308862.1:p.Val20983=
|
|
XM_024453095.1:c.62946T>A
(TTN)
|
XP_024308863.1:p.Val20982=
|
|
XM_024453096.1:c.62379T>A
(TTN)
|
XP_024308864.1:p.Val20793=
|
|
XM_024453097.1:c.59721T>A
(TTN)
|
XP_024308865.1:p.Val19907=
|
|
XM_024453098.1:c.59640T>A
(TTN)
|
XP_024308866.1:p.Val19880=
|
|
XM_024453099.1:c.41403T>A
(TTN)
|
XP_024308867.1:p.Val13801=
|
|
XM_024453100.1:c.31257T>A
(TTN)
|
XP_024308868.1:p.Val10419=
|
|