ENST00000342992.11:c.47750A>T
(TTN)
|
ENSP00000343764.6:p.Asp15917Val
|
|
ENST00000342175.11:c.28835A>T
(TTN)
|
ENSP00000340554.6:p.Asp9612Val
|
|
ENST00000359218.10:c.28634A>T
(TTN)
|
ENSP00000352154.5:p.Asp9545Val
|
|
ENST00000342175.10:c.28835A>T
(TTN)
|
ENSP00000340554.6:p.Asp9612Val
|
|
ENST00000342992.10:c.47750A>T
(TTN)
|
ENSP00000343764.6:p.Asp15917Val
|
|
ENST00000359218.9:c.28634A>T
(TTN)
|
ENSP00000352154.5:p.Asp9545Val
|
|
ENST00000460472.6:c.28259A>T
(TTN)
|
ENSP00000434586.1:p.Asp9420Val
|
|
ENST00000589042.5:c.55454A>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp18485Val
|
|
ENST00000591111.5:c.50531A>T
(TTN)
|
ENSP00000465570.1:p.Asp16844Val
|
|
ENST00000615779.4:c.50531A>T
(TTN)
|
ENSP00000483597.1:p.Asp16844Val
|
|
NM_001256850.1:c.50531A>T
(TTN)
|
NP_001243779.1:p.Asp16844Val
|
|
NM_001267550.2:c.55454A>T
(TTN)
MANE Select
|
NP_001254479.2:p.Asp18485Val
|
|
NM_003319.4:c.28259A>T
(TTN)
|
NP_003310.4:p.Asp9420Val
|
|
NM_133378.4:c.47750A>T
(TTN)
|
NP_596869.4:p.Asp15917Val
|
|
NM_133432.3:c.28634A>T
(TTN)
|
NP_597676.3:p.Asp9545Val
|
|
NM_133437.4:c.28835A>T
(TTN)
|
NP_597681.4:p.Asp9612Val
|
|
NR_038271.1:n.682+3862T>A
(TTN-AS1)
|
|
|
NR_038272.1:n.3917+876T>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.54551A>T
(TTN)
|
XP_011510031.1:p.Asp18184Val
|
|
XM_011511730.1:c.28445A>T
(TTN)
|
XP_011510032.1:p.Asp9482Val
|
|
XM_011511731.1:c.28304A>T
(TTN)
|
XP_011510033.1:p.Asp9435Val
|
|
XM_017004819.1:c.54347A>T
(TTN)
|
XP_016860308.1:p.Asp18116Val
|
|
XM_017004820.1:c.49745A>T
(TTN)
|
XP_016860309.1:p.Asp16582Val
|
|
XM_017004821.1:c.49742A>T
(TTN)
|
XP_016860310.1:p.Asp16581Val
|
|
XM_017004822.1:c.46784A>T
(TTN)
|
XP_016860311.1:p.Asp15595Val
|
|
XM_017004823.1:c.28400A>T
(TTN)
|
XP_016860312.1:p.Asp9467Val
|
|
XM_024453094.1:c.49895A>T
(TTN)
|
XP_024308862.1:p.Asp16632Val
|
|
XM_024453095.1:c.49892A>T
(TTN)
|
XP_024308863.1:p.Asp16631Val
|
|
XM_024453096.1:c.49325A>T
(TTN)
|
XP_024308864.1:p.Asp16442Val
|
|
XM_024453097.1:c.46667A>T
(TTN)
|
XP_024308865.1:p.Asp15556Val
|
|
XM_024453098.1:c.46586A>T
(TTN)
|
XP_024308866.1:p.Asp15529Val
|
|
XM_024453099.1:c.28349A>T
(TTN)
|
XP_024308867.1:p.Asp9450Val
|
|
XM_024453100.1:c.18203A>T
(TTN)
|
XP_024308868.1:p.Asp6068Val
|
|