ENST00000342992.11:c.98472T>G
(TTN)
|
ENSP00000343764.6:p.Thr32824=
|
|
ENST00000342175.11:c.79557T>G
(TTN)
|
ENSP00000340554.6:p.Thr26519=
|
|
ENST00000359218.10:c.79356T>G
(TTN)
|
ENSP00000352154.5:p.Thr26452=
|
|
ENST00000342175.10:c.79557T>G
(TTN)
|
ENSP00000340554.6:p.Thr26519=
|
|
ENST00000342992.10:c.98472T>G
(TTN)
|
ENSP00000343764.6:p.Thr32824=
|
|
ENST00000359218.9:c.79356T>G
(TTN)
|
ENSP00000352154.5:p.Thr26452=
|
|
ENST00000460472.6:c.78981T>G
(TTN)
|
ENSP00000434586.1:p.Thr26327=
|
|
ENST00000589042.5:c.106176T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr35392=
|
|
ENST00000591111.5:c.101253T>G
(TTN)
|
ENSP00000465570.1:p.Thr33751=
|
|
ENST00000615779.4:c.101253T>G
(TTN)
|
ENSP00000483597.1:p.Thr33751=
|
|
NM_001256850.1:c.101253T>G
(TTN)
|
NP_001243779.1:p.Thr33751=
|
|
NM_001267550.2:c.106176T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Thr35392=
|
|
NM_003319.4:c.78981T>G
(TTN)
|
NP_003310.4:p.Thr26327=
|
|
NM_133378.4:c.98472T>G
(TTN)
|
NP_596869.4:p.Thr32824=
|
|
NM_133432.3:c.79356T>G
(TTN)
|
NP_597676.3:p.Thr26452=
|
|
NM_133437.4:c.79557T>G
(TTN)
|
NP_597681.4:p.Thr26519=
|
|
NR_038271.1:n.446+6803A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5293A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.105273T>G
(TTN)
|
XP_011510031.1:p.Thr35091=
|
|
XM_011511730.1:c.79167T>G
(TTN)
|
XP_011510032.1:p.Thr26389=
|
|
XM_011511731.1:c.79026T>G
(TTN)
|
XP_011510033.1:p.Thr26342=
|
|
XM_017004819.1:c.105069T>G
(TTN)
|
XP_016860308.1:p.Thr35023=
|
|
XM_017004820.1:c.100467T>G
(TTN)
|
XP_016860309.1:p.Thr33489=
|
|
XM_017004821.1:c.100464T>G
(TTN)
|
XP_016860310.1:p.Thr33488=
|
|
XM_017004822.1:c.97506T>G
(TTN)
|
XP_016860311.1:p.Thr32502=
|
|
XM_017004823.1:c.79122T>G
(TTN)
|
XP_016860312.1:p.Thr26374=
|
|
XM_024453094.1:c.100617T>G
(TTN)
|
XP_024308862.1:p.Thr33539=
|
|
XM_024453095.1:c.100614T>G
(TTN)
|
XP_024308863.1:p.Thr33538=
|
|
XM_024453096.1:c.100047T>G
(TTN)
|
XP_024308864.1:p.Thr33349=
|
|
XM_024453097.1:c.97389T>G
(TTN)
|
XP_024308865.1:p.Thr32463=
|
|
XM_024453098.1:c.97308T>G
(TTN)
|
XP_024308866.1:p.Thr32436=
|
|
XM_024453099.1:c.79071T>G
(TTN)
|
XP_024308867.1:p.Thr26357=
|
|
XM_024453100.1:c.68925T>G
(TTN)
|
XP_024308868.1:p.Thr22975=
|
|