ENST00000342992.11:c.51629A>C
(TTN)
|
ENSP00000343764.6:p.Lys17210Thr
|
|
ENST00000342175.11:c.32714A>C
(TTN)
|
ENSP00000340554.6:p.Lys10905Thr
|
|
ENST00000359218.10:c.32513A>C
(TTN)
|
ENSP00000352154.5:p.Lys10838Thr
|
|
ENST00000342175.10:c.32714A>C
(TTN)
|
ENSP00000340554.6:p.Lys10905Thr
|
|
ENST00000342992.10:c.51629A>C
(TTN)
|
ENSP00000343764.6:p.Lys17210Thr
|
|
ENST00000359218.9:c.32513A>C
(TTN)
|
ENSP00000352154.5:p.Lys10838Thr
|
|
ENST00000460472.6:c.32138A>C
(TTN)
|
ENSP00000434586.1:p.Lys10713Thr
|
|
ENST00000589042.5:c.59333A>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Lys19778Thr
|
|
ENST00000591111.5:c.54410A>C
(TTN)
|
ENSP00000465570.1:p.Lys18137Thr
|
|
ENST00000615779.4:c.54410A>C
(TTN)
|
ENSP00000483597.1:p.Lys18137Thr
|
|
NM_001256850.1:c.54410A>C
(TTN)
|
NP_001243779.1:p.Lys18137Thr
|
|
NM_001267550.2:c.59333A>C
(TTN)
MANE Select
|
NP_001254479.2:p.Lys19778Thr
|
|
NM_003319.4:c.32138A>C
(TTN)
|
NP_003310.4:p.Lys10713Thr
|
|
NM_133378.4:c.51629A>C
(TTN)
|
NP_596869.4:p.Lys17210Thr
|
|
NM_133432.3:c.32513A>C
(TTN)
|
NP_597676.3:p.Lys10838Thr
|
|
NM_133437.4:c.32714A>C
(TTN)
|
NP_597681.4:p.Lys10905Thr
|
|
NR_038271.1:n.597-4810T>G
(TTN-AS1)
|
|
|
NR_038272.1:n.3364+1472T>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.58430A>C
(TTN)
|
XP_011510031.1:p.Lys19477Thr
|
|
XM_011511730.1:c.32324A>C
(TTN)
|
XP_011510032.1:p.Lys10775Thr
|
|
XM_011511731.1:c.32183A>C
(TTN)
|
XP_011510033.1:p.Lys10728Thr
|
|
XM_017004819.1:c.58226A>C
(TTN)
|
XP_016860308.1:p.Lys19409Thr
|
|
XM_017004820.1:c.53624A>C
(TTN)
|
XP_016860309.1:p.Lys17875Thr
|
|
XM_017004821.1:c.53621A>C
(TTN)
|
XP_016860310.1:p.Lys17874Thr
|
|
XM_017004822.1:c.50663A>C
(TTN)
|
XP_016860311.1:p.Lys16888Thr
|
|
XM_017004823.1:c.32279A>C
(TTN)
|
XP_016860312.1:p.Lys10760Thr
|
|
XM_024453094.1:c.53774A>C
(TTN)
|
XP_024308862.1:p.Lys17925Thr
|
|
XM_024453095.1:c.53771A>C
(TTN)
|
XP_024308863.1:p.Lys17924Thr
|
|
XM_024453096.1:c.53204A>C
(TTN)
|
XP_024308864.1:p.Lys17735Thr
|
|
XM_024453097.1:c.50546A>C
(TTN)
|
XP_024308865.1:p.Lys16849Thr
|
|
XM_024453098.1:c.50465A>C
(TTN)
|
XP_024308866.1:p.Lys16822Thr
|
|
XM_024453099.1:c.32228A>C
(TTN)
|
XP_024308867.1:p.Lys10743Thr
|
|
XM_024453100.1:c.22082A>C
(TTN)
|
XP_024308868.1:p.Lys7361Thr
|
|