ENST00000342992.11:c.82635T>A
(TTN)
|
ENSP00000343764.6:p.Asp27545Glu
|
|
ENST00000342175.11:c.63720T>A
(TTN)
|
ENSP00000340554.6:p.Asp21240Glu
|
|
ENST00000359218.10:c.63519T>A
(TTN)
|
ENSP00000352154.5:p.Asp21173Glu
|
|
ENST00000342175.10:c.63720T>A
(TTN)
|
ENSP00000340554.6:p.Asp21240Glu
|
|
ENST00000342992.10:c.82635T>A
(TTN)
|
ENSP00000343764.6:p.Asp27545Glu
|
|
ENST00000359218.9:c.63519T>A
(TTN)
|
ENSP00000352154.5:p.Asp21173Glu
|
|
ENST00000460472.6:c.63144T>A
(TTN)
|
ENSP00000434586.1:p.Asp21048Glu
|
|
ENST00000589042.5:c.90339T>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp30113Glu
|
|
ENST00000591111.5:c.85416T>A
(TTN)
|
ENSP00000465570.1:p.Asp28472Glu
|
|
ENST00000615779.4:c.85416T>A
(TTN)
|
ENSP00000483597.1:p.Asp28472Glu
|
|
NM_001256850.1:c.85416T>A
(TTN)
|
NP_001243779.1:p.Asp28472Glu
|
|
NM_001267550.2:c.90339T>A
(TTN)
MANE Select
|
NP_001254479.2:p.Asp30113Glu
|
|
NM_003319.4:c.63144T>A
(TTN)
|
NP_003310.4:p.Asp21048Glu
|
|
NM_133378.4:c.82635T>A
(TTN)
|
NP_596869.4:p.Asp27545Glu
|
|
NM_133432.3:c.63519T>A
(TTN)
|
NP_597676.3:p.Asp21173Glu
|
|
NM_133437.4:c.63720T>A
(TTN)
|
NP_597681.4:p.Asp21240Glu
|
|
NR_038271.1:n.447-18739A>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+10200A>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.89436T>A
(TTN)
|
XP_011510031.1:p.Asp29812Glu
|
|
XM_011511730.1:c.63330T>A
(TTN)
|
XP_011510032.1:p.Asp21110Glu
|
|
XM_011511731.1:c.63189T>A
(TTN)
|
XP_011510033.1:p.Asp21063Glu
|
|
XM_017004819.1:c.89232T>A
(TTN)
|
XP_016860308.1:p.Asp29744Glu
|
|
XM_017004820.1:c.84630T>A
(TTN)
|
XP_016860309.1:p.Asp28210Glu
|
|
XM_017004821.1:c.84627T>A
(TTN)
|
XP_016860310.1:p.Asp28209Glu
|
|
XM_017004822.1:c.81669T>A
(TTN)
|
XP_016860311.1:p.Asp27223Glu
|
|
XM_017004823.1:c.63285T>A
(TTN)
|
XP_016860312.1:p.Asp21095Glu
|
|
XM_024453094.1:c.84780T>A
(TTN)
|
XP_024308862.1:p.Asp28260Glu
|
|
XM_024453095.1:c.84777T>A
(TTN)
|
XP_024308863.1:p.Asp28259Glu
|
|
XM_024453096.1:c.84210T>A
(TTN)
|
XP_024308864.1:p.Asp28070Glu
|
|
XM_024453097.1:c.81552T>A
(TTN)
|
XP_024308865.1:p.Asp27184Glu
|
|
XM_024453098.1:c.81471T>A
(TTN)
|
XP_024308866.1:p.Asp27157Glu
|
|
XM_024453099.1:c.63234T>A
(TTN)
|
XP_024308867.1:p.Asp21078Glu
|
|
XM_024453100.1:c.53088T>A
(TTN)
|
XP_024308868.1:p.Asp17696Glu
|
|