ENST00000342992.11:c.98532T>G
(TTN)
|
ENSP00000343764.6:p.Ala32844=
|
|
ENST00000342175.11:c.79617T>G
(TTN)
|
ENSP00000340554.6:p.Ala26539=
|
|
ENST00000359218.10:c.79416T>G
(TTN)
|
ENSP00000352154.5:p.Ala26472=
|
|
ENST00000342175.10:c.79617T>G
(TTN)
|
ENSP00000340554.6:p.Ala26539=
|
|
ENST00000342992.10:c.98532T>G
(TTN)
|
ENSP00000343764.6:p.Ala32844=
|
|
ENST00000359218.9:c.79416T>G
(TTN)
|
ENSP00000352154.5:p.Ala26472=
|
|
ENST00000460472.6:c.79041T>G
(TTN)
|
ENSP00000434586.1:p.Ala26347=
|
|
ENST00000589042.5:c.106236T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ala35412=
|
|
ENST00000591111.5:c.101313T>G
(TTN)
|
ENSP00000465570.1:p.Ala33771=
|
|
ENST00000615779.4:c.101313T>G
(TTN)
|
ENSP00000483597.1:p.Ala33771=
|
|
NM_001256850.1:c.101313T>G
(TTN)
|
NP_001243779.1:p.Ala33771=
|
|
NM_001267550.2:c.106236T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Ala35412=
|
|
NM_003319.4:c.79041T>G
(TTN)
|
NP_003310.4:p.Ala26347=
|
|
NM_133378.4:c.98532T>G
(TTN)
|
NP_596869.4:p.Ala32844=
|
|
NM_133432.3:c.79416T>G
(TTN)
|
NP_597676.3:p.Ala26472=
|
|
NM_133437.4:c.79617T>G
(TTN)
|
NP_597681.4:p.Ala26539=
|
|
NR_038271.1:n.446+6743A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5353A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.105333T>G
(TTN)
|
XP_011510031.1:p.Ala35111=
|
|
XM_011511730.1:c.79227T>G
(TTN)
|
XP_011510032.1:p.Ala26409=
|
|
XM_011511731.1:c.79086T>G
(TTN)
|
XP_011510033.1:p.Ala26362=
|
|
XM_017004819.1:c.105129T>G
(TTN)
|
XP_016860308.1:p.Ala35043=
|
|
XM_017004820.1:c.100527T>G
(TTN)
|
XP_016860309.1:p.Ala33509=
|
|
XM_017004821.1:c.100524T>G
(TTN)
|
XP_016860310.1:p.Ala33508=
|
|
XM_017004822.1:c.97566T>G
(TTN)
|
XP_016860311.1:p.Ala32522=
|
|
XM_017004823.1:c.79182T>G
(TTN)
|
XP_016860312.1:p.Ala26394=
|
|
XM_024453094.1:c.100677T>G
(TTN)
|
XP_024308862.1:p.Ala33559=
|
|
XM_024453095.1:c.100674T>G
(TTN)
|
XP_024308863.1:p.Ala33558=
|
|
XM_024453096.1:c.100107T>G
(TTN)
|
XP_024308864.1:p.Ala33369=
|
|
XM_024453097.1:c.97449T>G
(TTN)
|
XP_024308865.1:p.Ala32483=
|
|
XM_024453098.1:c.97368T>G
(TTN)
|
XP_024308866.1:p.Ala32456=
|
|
XM_024453099.1:c.79131T>G
(TTN)
|
XP_024308867.1:p.Ala26377=
|
|
XM_024453100.1:c.68985T>G
(TTN)
|
XP_024308868.1:p.Ala22995=
|
|