ENST00000342992.11:c.91965T>G
(TTN)
|
ENSP00000343764.6:p.Arg30655=
|
|
ENST00000342175.11:c.73050T>G
(TTN)
|
ENSP00000340554.6:p.Arg24350=
|
|
ENST00000359218.10:c.72849T>G
(TTN)
|
ENSP00000352154.5:p.Arg24283=
|
|
ENST00000342175.10:c.73050T>G
(TTN)
|
ENSP00000340554.6:p.Arg24350=
|
|
ENST00000342992.10:c.91965T>G
(TTN)
|
ENSP00000343764.6:p.Arg30655=
|
|
ENST00000359218.9:c.72849T>G
(TTN)
|
ENSP00000352154.5:p.Arg24283=
|
|
ENST00000460472.6:c.72474T>G
(TTN)
|
ENSP00000434586.1:p.Arg24158=
|
|
ENST00000589042.5:c.99669T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Arg33223=
|
|
ENST00000591111.5:c.94746T>G
(TTN)
|
ENSP00000465570.1:p.Arg31582=
|
|
ENST00000615779.4:c.94746T>G
(TTN)
|
ENSP00000483597.1:p.Arg31582=
|
|
NM_001256850.1:c.94746T>G
(TTN)
|
NP_001243779.1:p.Arg31582=
|
|
NM_001267550.2:c.99669T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Arg33223=
|
|
NM_003319.4:c.72474T>G
(TTN)
|
NP_003310.4:p.Arg24158=
|
|
NM_133378.4:c.91965T>G
(TTN)
|
NP_596869.4:p.Arg30655=
|
|
NM_133432.3:c.72849T>G
(TTN)
|
NP_597676.3:p.Arg24283=
|
|
NM_133437.4:c.73050T>G
(TTN)
|
NP_597681.4:p.Arg24350=
|
|
NR_038271.1:n.446+13902A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.494A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.98766T>G
(TTN)
|
XP_011510031.1:p.Arg32922=
|
|
XM_011511730.1:c.72660T>G
(TTN)
|
XP_011510032.1:p.Arg24220=
|
|
XM_011511731.1:c.72519T>G
(TTN)
|
XP_011510033.1:p.Arg24173=
|
|
XM_017004819.1:c.98562T>G
(TTN)
|
XP_016860308.1:p.Arg32854=
|
|
XM_017004820.1:c.93960T>G
(TTN)
|
XP_016860309.1:p.Arg31320=
|
|
XM_017004821.1:c.93957T>G
(TTN)
|
XP_016860310.1:p.Arg31319=
|
|
XM_017004822.1:c.90999T>G
(TTN)
|
XP_016860311.1:p.Arg30333=
|
|
XM_017004823.1:c.72615T>G
(TTN)
|
XP_016860312.1:p.Arg24205=
|
|
XM_024453094.1:c.94110T>G
(TTN)
|
XP_024308862.1:p.Arg31370=
|
|
XM_024453095.1:c.94107T>G
(TTN)
|
XP_024308863.1:p.Arg31369=
|
|
XM_024453096.1:c.93540T>G
(TTN)
|
XP_024308864.1:p.Arg31180=
|
|
XM_024453097.1:c.90882T>G
(TTN)
|
XP_024308865.1:p.Arg30294=
|
|
XM_024453098.1:c.90801T>G
(TTN)
|
XP_024308866.1:p.Arg30267=
|
|
XM_024453099.1:c.72564T>G
(TTN)
|
XP_024308867.1:p.Arg24188=
|
|
XM_024453100.1:c.62418T>G
(TTN)
|
XP_024308868.1:p.Arg20806=
|
|