ENST00000342992.11:c.62601G>A
(TTN)
|
ENSP00000343764.6:p.Thr20867=
|
|
ENST00000342175.11:c.43686G>A
(TTN)
|
ENSP00000340554.6:p.Thr14562=
|
|
ENST00000359218.10:c.43485G>A
(TTN)
|
ENSP00000352154.5:p.Thr14495=
|
|
ENST00000342175.10:c.43686G>A
(TTN)
|
ENSP00000340554.6:p.Thr14562=
|
|
ENST00000342992.10:c.62601G>A
(TTN)
|
ENSP00000343764.6:p.Thr20867=
|
|
ENST00000359218.9:c.43485G>A
(TTN)
|
ENSP00000352154.5:p.Thr14495=
|
|
ENST00000460472.6:c.43110G>A
(TTN)
|
ENSP00000434586.1:p.Thr14370=
|
|
ENST00000589042.5:c.70305G>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr23435=
|
|
ENST00000591111.5:c.65382G>A
(TTN)
|
ENSP00000465570.1:p.Thr21794=
|
|
ENST00000615779.4:c.65382G>A
(TTN)
|
ENSP00000483597.1:p.Thr21794=
|
|
NM_001256850.1:c.65382G>A
(TTN)
|
NP_001243779.1:p.Thr21794=
|
|
NM_001267550.2:c.70305G>A
(TTN)
MANE Select
|
NP_001254479.2:p.Thr23435=
|
|
NM_003319.4:c.43110G>A
(TTN)
|
NP_003310.4:p.Thr14370=
|
|
NM_133378.4:c.62601G>A
(TTN)
|
NP_596869.4:p.Thr20867=
|
|
NM_133432.3:c.43485G>A
(TTN)
|
NP_597676.3:p.Thr14495=
|
|
NM_133437.4:c.43686G>A
(TTN)
|
NP_597681.4:p.Thr14562=
|
|
NR_038271.1:n.596+4378C>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-6745C>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.69402G>A
(TTN)
|
XP_011510031.1:p.Thr23134=
|
|
XM_011511730.1:c.43296G>A
(TTN)
|
XP_011510032.1:p.Thr14432=
|
|
XM_011511731.1:c.43155G>A
(TTN)
|
XP_011510033.1:p.Thr14385=
|
|
XM_017004819.1:c.69198G>A
(TTN)
|
XP_016860308.1:p.Thr23066=
|
|
XM_017004820.1:c.64596G>A
(TTN)
|
XP_016860309.1:p.Thr21532=
|
|
XM_017004821.1:c.64593G>A
(TTN)
|
XP_016860310.1:p.Thr21531=
|
|
XM_017004822.1:c.61635G>A
(TTN)
|
XP_016860311.1:p.Thr20545=
|
|
XM_017004823.1:c.43251G>A
(TTN)
|
XP_016860312.1:p.Thr14417=
|
|
XM_024453094.1:c.64746G>A
(TTN)
|
XP_024308862.1:p.Thr21582=
|
|
XM_024453095.1:c.64743G>A
(TTN)
|
XP_024308863.1:p.Thr21581=
|
|
XM_024453096.1:c.64176G>A
(TTN)
|
XP_024308864.1:p.Thr21392=
|
|
XM_024453097.1:c.61518G>A
(TTN)
|
XP_024308865.1:p.Thr20506=
|
|
XM_024453098.1:c.61437G>A
(TTN)
|
XP_024308866.1:p.Thr20479=
|
|
XM_024453099.1:c.43200G>A
(TTN)
|
XP_024308867.1:p.Thr14400=
|
|
XM_024453100.1:c.33054G>A
(TTN)
|
XP_024308868.1:p.Thr11018=
|
|