ENST00000342992.11:c.92328A>G
(TTN)
|
ENSP00000343764.6:p.Ser30776=
|
|
ENST00000342175.11:c.73413A>G
(TTN)
|
ENSP00000340554.6:p.Ser24471=
|
|
ENST00000359218.10:c.73212A>G
(TTN)
|
ENSP00000352154.5:p.Ser24404=
|
|
ENST00000342175.10:c.73413A>G
(TTN)
|
ENSP00000340554.6:p.Ser24471=
|
|
ENST00000342992.10:c.92328A>G
(TTN)
|
ENSP00000343764.6:p.Ser30776=
|
|
ENST00000359218.9:c.73212A>G
(TTN)
|
ENSP00000352154.5:p.Ser24404=
|
|
ENST00000460472.6:c.72837A>G
(TTN)
|
ENSP00000434586.1:p.Ser24279=
|
|
ENST00000589042.5:c.100032A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ser33344=
|
|
ENST00000591111.5:c.95109A>G
(TTN)
|
ENSP00000465570.1:p.Ser31703=
|
|
ENST00000615779.4:c.95109A>G
(TTN)
|
ENSP00000483597.1:p.Ser31703=
|
|
NM_001256850.1:c.95109A>G
(TTN)
|
NP_001243779.1:p.Ser31703=
|
|
NM_001267550.2:c.100032A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Ser33344=
|
|
NM_003319.4:c.72837A>G
(TTN)
|
NP_003310.4:p.Ser24279=
|
|
NM_133378.4:c.92328A>G
(TTN)
|
NP_596869.4:p.Ser30776=
|
|
NM_133432.3:c.73212A>G
(TTN)
|
NP_597676.3:p.Ser24404=
|
|
NM_133437.4:c.73413A>G
(TTN)
|
NP_597681.4:p.Ser24471=
|
|
NR_038271.1:n.446+13441T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.317-284T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.99129A>G
(TTN)
|
XP_011510031.1:p.Ser33043=
|
|
XM_011511730.1:c.73023A>G
(TTN)
|
XP_011510032.1:p.Ser24341=
|
|
XM_011511731.1:c.72882A>G
(TTN)
|
XP_011510033.1:p.Ser24294=
|
|
XM_017004819.1:c.98925A>G
(TTN)
|
XP_016860308.1:p.Ser32975=
|
|
XM_017004820.1:c.94323A>G
(TTN)
|
XP_016860309.1:p.Ser31441=
|
|
XM_017004821.1:c.94320A>G
(TTN)
|
XP_016860310.1:p.Ser31440=
|
|
XM_017004822.1:c.91362A>G
(TTN)
|
XP_016860311.1:p.Ser30454=
|
|
XM_017004823.1:c.72978A>G
(TTN)
|
XP_016860312.1:p.Ser24326=
|
|
XM_024453094.1:c.94473A>G
(TTN)
|
XP_024308862.1:p.Ser31491=
|
|
XM_024453095.1:c.94470A>G
(TTN)
|
XP_024308863.1:p.Ser31490=
|
|
XM_024453096.1:c.93903A>G
(TTN)
|
XP_024308864.1:p.Ser31301=
|
|
XM_024453097.1:c.91245A>G
(TTN)
|
XP_024308865.1:p.Ser30415=
|
|
XM_024453098.1:c.91164A>G
(TTN)
|
XP_024308866.1:p.Ser30388=
|
|
XM_024453099.1:c.72927A>G
(TTN)
|
XP_024308867.1:p.Ser24309=
|
|
XM_024453100.1:c.62781A>G
(TTN)
|
XP_024308868.1:p.Ser20927=
|
|