ENST00000342992.11:c.53088T>A
(TTN)
|
ENSP00000343764.6:p.Val17696=
|
|
ENST00000342175.11:c.34173T>A
(TTN)
|
ENSP00000340554.6:p.Val11391=
|
|
ENST00000359218.10:c.33972T>A
(TTN)
|
ENSP00000352154.5:p.Val11324=
|
|
ENST00000342175.10:c.34173T>A
(TTN)
|
ENSP00000340554.6:p.Val11391=
|
|
ENST00000342992.10:c.53088T>A
(TTN)
|
ENSP00000343764.6:p.Val17696=
|
|
ENST00000359218.9:c.33972T>A
(TTN)
|
ENSP00000352154.5:p.Val11324=
|
|
ENST00000460472.6:c.33597T>A
(TTN)
|
ENSP00000434586.1:p.Val11199=
|
|
ENST00000589042.5:c.60792T>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Val20264=
|
|
ENST00000591111.5:c.55869T>A
(TTN)
|
ENSP00000465570.1:p.Val18623=
|
|
ENST00000615779.4:c.55869T>A
(TTN)
|
ENSP00000483597.1:p.Val18623=
|
|
NM_001256850.1:c.55869T>A
(TTN)
|
NP_001243779.1:p.Val18623=
|
|
NM_001267550.2:c.60792T>A
(TTN)
MANE Select
|
NP_001254479.2:p.Val20264=
|
|
NM_003319.4:c.33597T>A
(TTN)
|
NP_003310.4:p.Val11199=
|
|
NM_133378.4:c.53088T>A
(TTN)
|
NP_596869.4:p.Val17696=
|
|
NM_133432.3:c.33972T>A
(TTN)
|
NP_597676.3:p.Val11324=
|
|
NM_133437.4:c.34173T>A
(TTN)
|
NP_597681.4:p.Val11391=
|
|
NR_038271.1:n.597-6663A>T
(TTN-AS1)
|
|
|
NR_038272.1:n.3189-206A>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.59889T>A
(TTN)
|
XP_011510031.1:p.Val19963=
|
|
XM_011511730.1:c.33783T>A
(TTN)
|
XP_011510032.1:p.Val11261=
|
|
XM_011511731.1:c.33642T>A
(TTN)
|
XP_011510033.1:p.Val11214=
|
|
XM_017004819.1:c.59685T>A
(TTN)
|
XP_016860308.1:p.Val19895=
|
|
XM_017004820.1:c.55083T>A
(TTN)
|
XP_016860309.1:p.Val18361=
|
|
XM_017004821.1:c.55080T>A
(TTN)
|
XP_016860310.1:p.Val18360=
|
|
XM_017004822.1:c.52122T>A
(TTN)
|
XP_016860311.1:p.Val17374=
|
|
XM_017004823.1:c.33738T>A
(TTN)
|
XP_016860312.1:p.Val11246=
|
|
XM_024453094.1:c.55233T>A
(TTN)
|
XP_024308862.1:p.Val18411=
|
|
XM_024453095.1:c.55230T>A
(TTN)
|
XP_024308863.1:p.Val18410=
|
|
XM_024453096.1:c.54663T>A
(TTN)
|
XP_024308864.1:p.Val18221=
|
|
XM_024453097.1:c.52005T>A
(TTN)
|
XP_024308865.1:p.Val17335=
|
|
XM_024453098.1:c.51924T>A
(TTN)
|
XP_024308866.1:p.Val17308=
|
|
XM_024453099.1:c.33687T>A
(TTN)
|
XP_024308867.1:p.Val11229=
|
|
XM_024453100.1:c.23541T>A
(TTN)
|
XP_024308868.1:p.Val7847=
|
|