ENST00000342992.11:c.98372G>T
(TTN)
|
ENSP00000343764.6:p.Cys32791Phe
|
|
ENST00000342175.11:c.79457G>T
(TTN)
|
ENSP00000340554.6:p.Cys26486Phe
|
|
ENST00000359218.10:c.79256G>T
(TTN)
|
ENSP00000352154.5:p.Cys26419Phe
|
|
ENST00000342175.10:c.79457G>T
(TTN)
|
ENSP00000340554.6:p.Cys26486Phe
|
|
ENST00000342992.10:c.98372G>T
(TTN)
|
ENSP00000343764.6:p.Cys32791Phe
|
|
ENST00000359218.9:c.79256G>T
(TTN)
|
ENSP00000352154.5:p.Cys26419Phe
|
|
ENST00000460472.6:c.78881G>T
(TTN)
|
ENSP00000434586.1:p.Cys26294Phe
|
|
ENST00000589042.5:c.106076G>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Cys35359Phe
|
|
ENST00000591111.5:c.101153G>T
(TTN)
|
ENSP00000465570.1:p.Cys33718Phe
|
|
ENST00000615779.4:c.101153G>T
(TTN)
|
ENSP00000483597.1:p.Cys33718Phe
|
|
NM_001256850.1:c.101153G>T
(TTN)
|
NP_001243779.1:p.Cys33718Phe
|
|
NM_001267550.2:c.106076G>T
(TTN)
MANE Select
|
NP_001254479.2:p.Cys35359Phe
|
|
NM_003319.4:c.78881G>T
(TTN)
|
NP_003310.4:p.Cys26294Phe
|
|
NM_133378.4:c.98372G>T
(TTN)
|
NP_596869.4:p.Cys32791Phe
|
|
NM_133432.3:c.79256G>T
(TTN)
|
NP_597676.3:p.Cys26419Phe
|
|
NM_133437.4:c.79457G>T
(TTN)
|
NP_597681.4:p.Cys26486Phe
|
|
NR_038271.1:n.446+6903C>A
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5193C>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.105173G>T
(TTN)
|
XP_011510031.1:p.Cys35058Phe
|
|
XM_011511730.1:c.79067G>T
(TTN)
|
XP_011510032.1:p.Cys26356Phe
|
|
XM_011511731.1:c.78926G>T
(TTN)
|
XP_011510033.1:p.Cys26309Phe
|
|
XM_017004819.1:c.104969G>T
(TTN)
|
XP_016860308.1:p.Cys34990Phe
|
|
XM_017004820.1:c.100367G>T
(TTN)
|
XP_016860309.1:p.Cys33456Phe
|
|
XM_017004821.1:c.100364G>T
(TTN)
|
XP_016860310.1:p.Cys33455Phe
|
|
XM_017004822.1:c.97406G>T
(TTN)
|
XP_016860311.1:p.Cys32469Phe
|
|
XM_017004823.1:c.79022G>T
(TTN)
|
XP_016860312.1:p.Cys26341Phe
|
|
XM_024453094.1:c.100517G>T
(TTN)
|
XP_024308862.1:p.Cys33506Phe
|
|
XM_024453095.1:c.100514G>T
(TTN)
|
XP_024308863.1:p.Cys33505Phe
|
|
XM_024453096.1:c.99947G>T
(TTN)
|
XP_024308864.1:p.Cys33316Phe
|
|
XM_024453097.1:c.97289G>T
(TTN)
|
XP_024308865.1:p.Cys32430Phe
|
|
XM_024453098.1:c.97208G>T
(TTN)
|
XP_024308866.1:p.Cys32403Phe
|
|
XM_024453099.1:c.78971G>T
(TTN)
|
XP_024308867.1:p.Cys26324Phe
|
|
XM_024453100.1:c.68825G>T
(TTN)
|
XP_024308868.1:p.Cys22942Phe
|
|