ENST00000342992.11:c.52265A>G
(TTN)
|
ENSP00000343764.6:p.Asp17422Gly
|
|
ENST00000342175.11:c.33350A>G
(TTN)
|
ENSP00000340554.6:p.Asp11117Gly
|
|
ENST00000359218.10:c.33149A>G
(TTN)
|
ENSP00000352154.5:p.Asp11050Gly
|
|
ENST00000342175.10:c.33350A>G
(TTN)
|
ENSP00000340554.6:p.Asp11117Gly
|
|
ENST00000342992.10:c.52265A>G
(TTN)
|
ENSP00000343764.6:p.Asp17422Gly
|
|
ENST00000359218.9:c.33149A>G
(TTN)
|
ENSP00000352154.5:p.Asp11050Gly
|
|
ENST00000460472.6:c.32774A>G
(TTN)
|
ENSP00000434586.1:p.Asp10925Gly
|
|
ENST00000589042.5:c.59969A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp19990Gly
|
|
ENST00000591111.5:c.55046A>G
(TTN)
|
ENSP00000465570.1:p.Asp18349Gly
|
|
ENST00000615779.4:c.55046A>G
(TTN)
|
ENSP00000483597.1:p.Asp18349Gly
|
|
NM_001256850.1:c.55046A>G
(TTN)
|
NP_001243779.1:p.Asp18349Gly
|
|
NM_001267550.2:c.59969A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Asp19990Gly
|
|
NM_003319.4:c.32774A>G
(TTN)
|
NP_003310.4:p.Asp10925Gly
|
|
NM_133378.4:c.52265A>G
(TTN)
|
NP_596869.4:p.Asp17422Gly
|
|
NM_133432.3:c.33149A>G
(TTN)
|
NP_597676.3:p.Asp11050Gly
|
|
NM_133437.4:c.33350A>G
(TTN)
|
NP_597681.4:p.Asp11117Gly
|
|
NR_038271.1:n.597-5746T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.3364+536T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.59066A>G
(TTN)
|
XP_011510031.1:p.Asp19689Gly
|
|
XM_011511730.1:c.32960A>G
(TTN)
|
XP_011510032.1:p.Asp10987Gly
|
|
XM_011511731.1:c.32819A>G
(TTN)
|
XP_011510033.1:p.Asp10940Gly
|
|
XM_017004819.1:c.58862A>G
(TTN)
|
XP_016860308.1:p.Asp19621Gly
|
|
XM_017004820.1:c.54260A>G
(TTN)
|
XP_016860309.1:p.Asp18087Gly
|
|
XM_017004821.1:c.54257A>G
(TTN)
|
XP_016860310.1:p.Asp18086Gly
|
|
XM_017004822.1:c.51299A>G
(TTN)
|
XP_016860311.1:p.Asp17100Gly
|
|
XM_017004823.1:c.32915A>G
(TTN)
|
XP_016860312.1:p.Asp10972Gly
|
|
XM_024453094.1:c.54410A>G
(TTN)
|
XP_024308862.1:p.Asp18137Gly
|
|
XM_024453095.1:c.54407A>G
(TTN)
|
XP_024308863.1:p.Asp18136Gly
|
|
XM_024453096.1:c.53840A>G
(TTN)
|
XP_024308864.1:p.Asp17947Gly
|
|
XM_024453097.1:c.51182A>G
(TTN)
|
XP_024308865.1:p.Asp17061Gly
|
|
XM_024453098.1:c.51101A>G
(TTN)
|
XP_024308866.1:p.Asp17034Gly
|
|
XM_024453099.1:c.32864A>G
(TTN)
|
XP_024308867.1:p.Asp10955Gly
|
|
XM_024453100.1:c.22718A>G
(TTN)
|
XP_024308868.1:p.Asp7573Gly
|
|