ENST00000342992.11:c.81309A>G
(TTN)
|
ENSP00000343764.6:p.Glu27103=
|
|
ENST00000342175.11:c.62394A>G
(TTN)
|
ENSP00000340554.6:p.Glu20798=
|
|
ENST00000359218.10:c.62193A>G
(TTN)
|
ENSP00000352154.5:p.Glu20731=
|
|
ENST00000342175.10:c.62394A>G
(TTN)
|
ENSP00000340554.6:p.Glu20798=
|
|
ENST00000342992.10:c.81309A>G
(TTN)
|
ENSP00000343764.6:p.Glu27103=
|
|
ENST00000359218.9:c.62193A>G
(TTN)
|
ENSP00000352154.5:p.Glu20731=
|
|
ENST00000460472.6:c.61818A>G
(TTN)
|
ENSP00000434586.1:p.Glu20606=
|
|
ENST00000589042.5:c.89013A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu29671=
|
|
ENST00000591111.5:c.84090A>G
(TTN)
|
ENSP00000465570.1:p.Glu28030=
|
|
ENST00000615779.4:c.84090A>G
(TTN)
|
ENSP00000483597.1:p.Glu28030=
|
|
NM_001256850.1:c.84090A>G
(TTN)
|
NP_001243779.1:p.Glu28030=
|
|
NM_001267550.2:c.89013A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Glu29671=
|
|
NM_003319.4:c.61818A>G
(TTN)
|
NP_003310.4:p.Glu20606=
|
|
NM_133378.4:c.81309A>G
(TTN)
|
NP_596869.4:p.Glu27103=
|
|
NM_133432.3:c.62193A>G
(TTN)
|
NP_597676.3:p.Glu20731=
|
|
NM_133437.4:c.62394A>G
(TTN)
|
NP_597681.4:p.Glu20798=
|
|
NR_038271.1:n.447-17202T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+11737T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.88110A>G
(TTN)
|
XP_011510031.1:p.Glu29370=
|
|
XM_011511730.1:c.62004A>G
(TTN)
|
XP_011510032.1:p.Glu20668=
|
|
XM_011511731.1:c.61863A>G
(TTN)
|
XP_011510033.1:p.Glu20621=
|
|
XM_017004819.1:c.87906A>G
(TTN)
|
XP_016860308.1:p.Glu29302=
|
|
XM_017004820.1:c.83304A>G
(TTN)
|
XP_016860309.1:p.Glu27768=
|
|
XM_017004821.1:c.83301A>G
(TTN)
|
XP_016860310.1:p.Glu27767=
|
|
XM_017004822.1:c.80343A>G
(TTN)
|
XP_016860311.1:p.Glu26781=
|
|
XM_017004823.1:c.61959A>G
(TTN)
|
XP_016860312.1:p.Glu20653=
|
|
XM_024453094.1:c.83454A>G
(TTN)
|
XP_024308862.1:p.Glu27818=
|
|
XM_024453095.1:c.83451A>G
(TTN)
|
XP_024308863.1:p.Glu27817=
|
|
XM_024453096.1:c.82884A>G
(TTN)
|
XP_024308864.1:p.Glu27628=
|
|
XM_024453097.1:c.80226A>G
(TTN)
|
XP_024308865.1:p.Glu26742=
|
|
XM_024453098.1:c.80145A>G
(TTN)
|
XP_024308866.1:p.Glu26715=
|
|
XM_024453099.1:c.61908A>G
(TTN)
|
XP_024308867.1:p.Glu20636=
|
|
XM_024453100.1:c.51762A>G
(TTN)
|
XP_024308868.1:p.Glu17254=
|
|