ENST00000342992.11:c.96638A>G
(TTN)
|
ENSP00000343764.6:p.Gln32213Arg
|
|
ENST00000342175.11:c.77723A>G
(TTN)
|
ENSP00000340554.6:p.Gln25908Arg
|
|
ENST00000359218.10:c.77522A>G
(TTN)
|
ENSP00000352154.5:p.Gln25841Arg
|
|
ENST00000342175.10:c.77723A>G
(TTN)
|
ENSP00000340554.6:p.Gln25908Arg
|
|
ENST00000342992.10:c.96638A>G
(TTN)
|
ENSP00000343764.6:p.Gln32213Arg
|
|
ENST00000359218.9:c.77522A>G
(TTN)
|
ENSP00000352154.5:p.Gln25841Arg
|
|
ENST00000460472.6:c.77147A>G
(TTN)
|
ENSP00000434586.1:p.Gln25716Arg
|
|
ENST00000589042.5:c.104342A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gln34781Arg
|
|
ENST00000591111.5:c.99419A>G
(TTN)
|
ENSP00000465570.1:p.Gln33140Arg
|
|
ENST00000615779.4:c.99419A>G
(TTN)
|
ENSP00000483597.1:p.Gln33140Arg
|
|
NM_001256850.1:c.99419A>G
(TTN)
|
NP_001243779.1:p.Gln33140Arg
|
|
NM_001267550.2:c.104342A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Gln34781Arg
|
|
NM_003319.4:c.77147A>G
(TTN)
|
NP_003310.4:p.Gln25716Arg
|
|
NM_133378.4:c.96638A>G
(TTN)
|
NP_596869.4:p.Gln32213Arg
|
|
NM_133432.3:c.77522A>G
(TTN)
|
NP_597676.3:p.Gln25841Arg
|
|
NM_133437.4:c.77723A>G
(TTN)
|
NP_597681.4:p.Gln25908Arg
|
|
NR_038271.1:n.446+8637T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3459T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.103439A>G
(TTN)
|
XP_011510031.1:p.Gln34480Arg
|
|
XM_011511730.1:c.77333A>G
(TTN)
|
XP_011510032.1:p.Gln25778Arg
|
|
XM_011511731.1:c.77192A>G
(TTN)
|
XP_011510033.1:p.Gln25731Arg
|
|
XM_017004819.1:c.103235A>G
(TTN)
|
XP_016860308.1:p.Gln34412Arg
|
|
XM_017004820.1:c.98633A>G
(TTN)
|
XP_016860309.1:p.Gln32878Arg
|
|
XM_017004821.1:c.98630A>G
(TTN)
|
XP_016860310.1:p.Gln32877Arg
|
|
XM_017004822.1:c.95672A>G
(TTN)
|
XP_016860311.1:p.Gln31891Arg
|
|
XM_017004823.1:c.77288A>G
(TTN)
|
XP_016860312.1:p.Gln25763Arg
|
|
XM_024453094.1:c.98783A>G
(TTN)
|
XP_024308862.1:p.Gln32928Arg
|
|
XM_024453095.1:c.98780A>G
(TTN)
|
XP_024308863.1:p.Gln32927Arg
|
|
XM_024453096.1:c.98213A>G
(TTN)
|
XP_024308864.1:p.Gln32738Arg
|
|
XM_024453097.1:c.95555A>G
(TTN)
|
XP_024308865.1:p.Gln31852Arg
|
|
XM_024453098.1:c.95474A>G
(TTN)
|
XP_024308866.1:p.Gln31825Arg
|
|
XM_024453099.1:c.77237A>G
(TTN)
|
XP_024308867.1:p.Gln25746Arg
|
|
XM_024453100.1:c.67091A>G
(TTN)
|
XP_024308868.1:p.Gln22364Arg
|
|