ENST00000342992.11:c.87102T>C
(TTN)
|
ENSP00000343764.6:p.Pro29034=
|
|
ENST00000342175.11:c.68187T>C
(TTN)
|
ENSP00000340554.6:p.Pro22729=
|
|
ENST00000359218.10:c.67986T>C
(TTN)
|
ENSP00000352154.5:p.Pro22662=
|
|
ENST00000342175.10:c.68187T>C
(TTN)
|
ENSP00000340554.6:p.Pro22729=
|
|
ENST00000342992.10:c.87102T>C
(TTN)
|
ENSP00000343764.6:p.Pro29034=
|
|
ENST00000359218.9:c.67986T>C
(TTN)
|
ENSP00000352154.5:p.Pro22662=
|
|
ENST00000460472.6:c.67611T>C
(TTN)
|
ENSP00000434586.1:p.Pro22537=
|
|
ENST00000589042.5:c.94806T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Pro31602=
|
|
ENST00000591111.5:c.89883T>C
(TTN)
|
ENSP00000465570.1:p.Pro29961=
|
|
ENST00000615779.4:c.89883T>C
(TTN)
|
ENSP00000483597.1:p.Pro29961=
|
|
NM_001256850.1:c.89883T>C
(TTN)
|
NP_001243779.1:p.Pro29961=
|
|
NM_001267550.2:c.94806T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Pro31602=
|
|
NM_003319.4:c.67611T>C
(TTN)
|
NP_003310.4:p.Pro22537=
|
|
NM_133378.4:c.87102T>C
(TTN)
|
NP_596869.4:p.Pro29034=
|
|
NM_133432.3:c.67986T>C
(TTN)
|
NP_597676.3:p.Pro22662=
|
|
NM_133437.4:c.68187T>C
(TTN)
|
NP_597681.4:p.Pro22729=
|
|
NR_038271.1:n.446+22986A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+4261A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.93903T>C
(TTN)
|
XP_011510031.1:p.Pro31301=
|
|
XM_011511730.1:c.67797T>C
(TTN)
|
XP_011510032.1:p.Pro22599=
|
|
XM_011511731.1:c.67656T>C
(TTN)
|
XP_011510033.1:p.Pro22552=
|
|
XM_017004819.1:c.93699T>C
(TTN)
|
XP_016860308.1:p.Pro31233=
|
|
XM_017004820.1:c.89097T>C
(TTN)
|
XP_016860309.1:p.Pro29699=
|
|
XM_017004821.1:c.89094T>C
(TTN)
|
XP_016860310.1:p.Pro29698=
|
|
XM_017004822.1:c.86136T>C
(TTN)
|
XP_016860311.1:p.Pro28712=
|
|
XM_017004823.1:c.67752T>C
(TTN)
|
XP_016860312.1:p.Pro22584=
|
|
XM_024453094.1:c.89247T>C
(TTN)
|
XP_024308862.1:p.Pro29749=
|
|
XM_024453095.1:c.89244T>C
(TTN)
|
XP_024308863.1:p.Pro29748=
|
|
XM_024453096.1:c.88677T>C
(TTN)
|
XP_024308864.1:p.Pro29559=
|
|
XM_024453097.1:c.86019T>C
(TTN)
|
XP_024308865.1:p.Pro28673=
|
|
XM_024453098.1:c.85938T>C
(TTN)
|
XP_024308866.1:p.Pro28646=
|
|
XM_024453099.1:c.67701T>C
(TTN)
|
XP_024308867.1:p.Pro22567=
|
|
XM_024453100.1:c.57555T>C
(TTN)
|
XP_024308868.1:p.Pro19185=
|
|