ENST00000342992.11:c.52893T>A
(TTN)
|
ENSP00000343764.6:p.Asp17631Glu
|
|
ENST00000342175.11:c.33978T>A
(TTN)
|
ENSP00000340554.6:p.Asp11326Glu
|
|
ENST00000359218.10:c.33777T>A
(TTN)
|
ENSP00000352154.5:p.Asp11259Glu
|
|
ENST00000342175.10:c.33978T>A
(TTN)
|
ENSP00000340554.6:p.Asp11326Glu
|
|
ENST00000342992.10:c.52893T>A
(TTN)
|
ENSP00000343764.6:p.Asp17631Glu
|
|
ENST00000359218.9:c.33777T>A
(TTN)
|
ENSP00000352154.5:p.Asp11259Glu
|
|
ENST00000460472.6:c.33402T>A
(TTN)
|
ENSP00000434586.1:p.Asp11134Glu
|
|
ENST00000589042.5:c.60597T>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp20199Glu
|
|
ENST00000591111.5:c.55674T>A
(TTN)
|
ENSP00000465570.1:p.Asp18558Glu
|
|
ENST00000615779.4:c.55674T>A
(TTN)
|
ENSP00000483597.1:p.Asp18558Glu
|
|
NM_001256850.1:c.55674T>A
(TTN)
|
NP_001243779.1:p.Asp18558Glu
|
|
NM_001267550.2:c.60597T>A
(TTN)
MANE Select
|
NP_001254479.2:p.Asp20199Glu
|
|
NM_003319.4:c.33402T>A
(TTN)
|
NP_003310.4:p.Asp11134Glu
|
|
NM_133378.4:c.52893T>A
(TTN)
|
NP_596869.4:p.Asp17631Glu
|
|
NM_133432.3:c.33777T>A
(TTN)
|
NP_597676.3:p.Asp11259Glu
|
|
NM_133437.4:c.33978T>A
(TTN)
|
NP_597681.4:p.Asp11326Glu
|
|
NR_038271.1:n.597-6468A>T
(TTN-AS1)
|
|
|
NR_038272.1:n.3189-11A>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.59694T>A
(TTN)
|
XP_011510031.1:p.Asp19898Glu
|
|
XM_011511730.1:c.33588T>A
(TTN)
|
XP_011510032.1:p.Asp11196Glu
|
|
XM_011511731.1:c.33447T>A
(TTN)
|
XP_011510033.1:p.Asp11149Glu
|
|
XM_017004819.1:c.59490T>A
(TTN)
|
XP_016860308.1:p.Asp19830Glu
|
|
XM_017004820.1:c.54888T>A
(TTN)
|
XP_016860309.1:p.Asp18296Glu
|
|
XM_017004821.1:c.54885T>A
(TTN)
|
XP_016860310.1:p.Asp18295Glu
|
|
XM_017004822.1:c.51927T>A
(TTN)
|
XP_016860311.1:p.Asp17309Glu
|
|
XM_017004823.1:c.33543T>A
(TTN)
|
XP_016860312.1:p.Asp11181Glu
|
|
XM_024453094.1:c.55038T>A
(TTN)
|
XP_024308862.1:p.Asp18346Glu
|
|
XM_024453095.1:c.55035T>A
(TTN)
|
XP_024308863.1:p.Asp18345Glu
|
|
XM_024453096.1:c.54468T>A
(TTN)
|
XP_024308864.1:p.Asp18156Glu
|
|
XM_024453097.1:c.51810T>A
(TTN)
|
XP_024308865.1:p.Asp17270Glu
|
|
XM_024453098.1:c.51729T>A
(TTN)
|
XP_024308866.1:p.Asp17243Glu
|
|
XM_024453099.1:c.33492T>A
(TTN)
|
XP_024308867.1:p.Asp11164Glu
|
|
XM_024453100.1:c.23346T>A
(TTN)
|
XP_024308868.1:p.Asp7782Glu
|
|