ENST00000342992.11:c.39532A>G
(TTN)
|
ENSP00000343764.6:p.Thr13178Ala
|
|
ENST00000342175.11:c.20617A>G
(TTN)
|
ENSP00000340554.6:p.Thr6873Ala
|
|
ENST00000359218.10:c.20416A>G
(TTN)
|
ENSP00000352154.5:p.Thr6806Ala
|
|
ENST00000342175.10:c.20617A>G
(TTN)
|
ENSP00000340554.6:p.Thr6873Ala
|
|
ENST00000342992.10:c.39532A>G
(TTN)
|
ENSP00000343764.6:p.Thr13178Ala
|
|
ENST00000359218.9:c.20416A>G
(TTN)
|
ENSP00000352154.5:p.Thr6806Ala
|
|
ENST00000460472.6:c.20041A>G
(TTN)
|
ENSP00000434586.1:p.Thr6681Ala
|
|
ENST00000589042.5:c.47236A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr15746Ala
|
|
ENST00000591111.5:c.42313A>G
(TTN)
|
ENSP00000465570.1:p.Thr14105Ala
|
|
ENST00000615779.4:c.42313A>G
(TTN)
|
ENSP00000483597.1:p.Thr14105Ala
|
|
NM_001256850.1:c.42313A>G
(TTN)
|
NP_001243779.1:p.Thr14105Ala
|
|
NM_001267550.2:c.47236A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Thr15746Ala
|
|
NM_003319.4:c.20041A>G
(TTN)
|
NP_003310.4:p.Thr6681Ala
|
|
NM_133378.4:c.39532A>G
(TTN)
|
NP_596869.4:p.Thr13178Ala
|
|
NM_133432.3:c.20416A>G
(TTN)
|
NP_597676.3:p.Thr6806Ala
|
|
NM_133437.4:c.20617A>G
(TTN)
|
NP_597681.4:p.Thr6873Ala
|
|
NR_038271.1:n.1605-1531T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.46333A>G
(TTN)
|
XP_011510031.1:p.Thr15445Ala
|
|
XM_011511730.1:c.20227A>G
(TTN)
|
XP_011510032.1:p.Thr6743Ala
|
|
XM_011511731.1:c.20086A>G
(TTN)
|
XP_011510033.1:p.Thr6696Ala
|
|
XM_017004819.1:c.46129A>G
(TTN)
|
XP_016860308.1:p.Thr15377Ala
|
|
XM_017004820.1:c.41527A>G
(TTN)
|
XP_016860309.1:p.Thr13843Ala
|
|
XM_017004821.1:c.41524A>G
(TTN)
|
XP_016860310.1:p.Thr13842Ala
|
|
XM_017004822.1:c.38566A>G
(TTN)
|
XP_016860311.1:p.Thr12856Ala
|
|
XM_017004823.1:c.20182A>G
(TTN)
|
XP_016860312.1:p.Thr6728Ala
|
|
XM_024453094.1:c.41677A>G
(TTN)
|
XP_024308862.1:p.Thr13893Ala
|
|
XM_024453095.1:c.41674A>G
(TTN)
|
XP_024308863.1:p.Thr13892Ala
|
|
XM_024453096.1:c.41107A>G
(TTN)
|
XP_024308864.1:p.Thr13703Ala
|
|
XM_024453097.1:c.38449A>G
(TTN)
|
XP_024308865.1:p.Thr12817Ala
|
|
XM_024453098.1:c.38368A>G
(TTN)
|
XP_024308866.1:p.Thr12790Ala
|
|
XM_024453099.1:c.20131A>G
(TTN)
|
XP_024308867.1:p.Thr6711Ala
|
|
XM_024453100.1:c.9985A>G
(TTN)
|
XP_024308868.1:p.Thr3329Ala
|
|