ENST00000342992.11:c.53086G>T
(TTN)
|
ENSP00000343764.6:p.Val17696Phe
|
|
ENST00000342175.11:c.34171G>T
(TTN)
|
ENSP00000340554.6:p.Val11391Phe
|
|
ENST00000359218.10:c.33970G>T
(TTN)
|
ENSP00000352154.5:p.Val11324Phe
|
|
ENST00000342175.10:c.34171G>T
(TTN)
|
ENSP00000340554.6:p.Val11391Phe
|
|
ENST00000342992.10:c.53086G>T
(TTN)
|
ENSP00000343764.6:p.Val17696Phe
|
|
ENST00000359218.9:c.33970G>T
(TTN)
|
ENSP00000352154.5:p.Val11324Phe
|
|
ENST00000460472.6:c.33595G>T
(TTN)
|
ENSP00000434586.1:p.Val11199Phe
|
|
ENST00000589042.5:c.60790G>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Val20264Phe
|
|
ENST00000591111.5:c.55867G>T
(TTN)
|
ENSP00000465570.1:p.Val18623Phe
|
|
ENST00000615779.4:c.55867G>T
(TTN)
|
ENSP00000483597.1:p.Val18623Phe
|
|
NM_001256850.1:c.55867G>T
(TTN)
|
NP_001243779.1:p.Val18623Phe
|
|
NM_001267550.2:c.60790G>T
(TTN)
MANE Select
|
NP_001254479.2:p.Val20264Phe
|
|
NM_003319.4:c.33595G>T
(TTN)
|
NP_003310.4:p.Val11199Phe
|
|
NM_133378.4:c.53086G>T
(TTN)
|
NP_596869.4:p.Val17696Phe
|
|
NM_133432.3:c.33970G>T
(TTN)
|
NP_597676.3:p.Val11324Phe
|
|
NM_133437.4:c.34171G>T
(TTN)
|
NP_597681.4:p.Val11391Phe
|
|
NR_038271.1:n.597-6661C>A
(TTN-AS1)
|
|
|
NR_038272.1:n.3189-204C>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.59887G>T
(TTN)
|
XP_011510031.1:p.Val19963Phe
|
|
XM_011511730.1:c.33781G>T
(TTN)
|
XP_011510032.1:p.Val11261Phe
|
|
XM_011511731.1:c.33640G>T
(TTN)
|
XP_011510033.1:p.Val11214Phe
|
|
XM_017004819.1:c.59683G>T
(TTN)
|
XP_016860308.1:p.Val19895Phe
|
|
XM_017004820.1:c.55081G>T
(TTN)
|
XP_016860309.1:p.Val18361Phe
|
|
XM_017004821.1:c.55078G>T
(TTN)
|
XP_016860310.1:p.Val18360Phe
|
|
XM_017004822.1:c.52120G>T
(TTN)
|
XP_016860311.1:p.Val17374Phe
|
|
XM_017004823.1:c.33736G>T
(TTN)
|
XP_016860312.1:p.Val11246Phe
|
|
XM_024453094.1:c.55231G>T
(TTN)
|
XP_024308862.1:p.Val18411Phe
|
|
XM_024453095.1:c.55228G>T
(TTN)
|
XP_024308863.1:p.Val18410Phe
|
|
XM_024453096.1:c.54661G>T
(TTN)
|
XP_024308864.1:p.Val18221Phe
|
|
XM_024453097.1:c.52003G>T
(TTN)
|
XP_024308865.1:p.Val17335Phe
|
|
XM_024453098.1:c.51922G>T
(TTN)
|
XP_024308866.1:p.Val17308Phe
|
|
XM_024453099.1:c.33685G>T
(TTN)
|
XP_024308867.1:p.Val11229Phe
|
|
XM_024453100.1:c.23539G>T
(TTN)
|
XP_024308868.1:p.Val7847Phe
|
|