ENST00000342992.11:c.82515T>G
(TTN)
|
ENSP00000343764.6:p.Gly27505=
|
|
ENST00000342175.11:c.63600T>G
(TTN)
|
ENSP00000340554.6:p.Gly21200=
|
|
ENST00000359218.10:c.63399T>G
(TTN)
|
ENSP00000352154.5:p.Gly21133=
|
|
ENST00000342175.10:c.63600T>G
(TTN)
|
ENSP00000340554.6:p.Gly21200=
|
|
ENST00000342992.10:c.82515T>G
(TTN)
|
ENSP00000343764.6:p.Gly27505=
|
|
ENST00000359218.9:c.63399T>G
(TTN)
|
ENSP00000352154.5:p.Gly21133=
|
|
ENST00000460472.6:c.63024T>G
(TTN)
|
ENSP00000434586.1:p.Gly21008=
|
|
ENST00000589042.5:c.90219T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gly30073=
|
|
ENST00000591111.5:c.85296T>G
(TTN)
|
ENSP00000465570.1:p.Gly28432=
|
|
ENST00000615779.4:c.85296T>G
(TTN)
|
ENSP00000483597.1:p.Gly28432=
|
|
NM_001256850.1:c.85296T>G
(TTN)
|
NP_001243779.1:p.Gly28432=
|
|
NM_001267550.2:c.90219T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Gly30073=
|
|
NM_003319.4:c.63024T>G
(TTN)
|
NP_003310.4:p.Gly21008=
|
|
NM_133378.4:c.82515T>G
(TTN)
|
NP_596869.4:p.Gly27505=
|
|
NM_133432.3:c.63399T>G
(TTN)
|
NP_597676.3:p.Gly21133=
|
|
NM_133437.4:c.63600T>G
(TTN)
|
NP_597681.4:p.Gly21200=
|
|
NR_038271.1:n.447-18619A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+10320A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.89316T>G
(TTN)
|
XP_011510031.1:p.Gly29772=
|
|
XM_011511730.1:c.63210T>G
(TTN)
|
XP_011510032.1:p.Gly21070=
|
|
XM_011511731.1:c.63069T>G
(TTN)
|
XP_011510033.1:p.Gly21023=
|
|
XM_017004819.1:c.89112T>G
(TTN)
|
XP_016860308.1:p.Gly29704=
|
|
XM_017004820.1:c.84510T>G
(TTN)
|
XP_016860309.1:p.Gly28170=
|
|
XM_017004821.1:c.84507T>G
(TTN)
|
XP_016860310.1:p.Gly28169=
|
|
XM_017004822.1:c.81549T>G
(TTN)
|
XP_016860311.1:p.Gly27183=
|
|
XM_017004823.1:c.63165T>G
(TTN)
|
XP_016860312.1:p.Gly21055=
|
|
XM_024453094.1:c.84660T>G
(TTN)
|
XP_024308862.1:p.Gly28220=
|
|
XM_024453095.1:c.84657T>G
(TTN)
|
XP_024308863.1:p.Gly28219=
|
|
XM_024453096.1:c.84090T>G
(TTN)
|
XP_024308864.1:p.Gly28030=
|
|
XM_024453097.1:c.81432T>G
(TTN)
|
XP_024308865.1:p.Gly27144=
|
|
XM_024453098.1:c.81351T>G
(TTN)
|
XP_024308866.1:p.Gly27117=
|
|
XM_024453099.1:c.63114T>G
(TTN)
|
XP_024308867.1:p.Gly21038=
|
|
XM_024453100.1:c.52968T>G
(TTN)
|
XP_024308868.1:p.Gly17656=
|
|