ENST00000342992.11:c.96750A>C
(TTN)
|
ENSP00000343764.6:p.Glu32250Asp
|
|
ENST00000342175.11:c.77835A>C
(TTN)
|
ENSP00000340554.6:p.Glu25945Asp
|
|
ENST00000359218.10:c.77634A>C
(TTN)
|
ENSP00000352154.5:p.Glu25878Asp
|
|
ENST00000342175.10:c.77835A>C
(TTN)
|
ENSP00000340554.6:p.Glu25945Asp
|
|
ENST00000342992.10:c.96750A>C
(TTN)
|
ENSP00000343764.6:p.Glu32250Asp
|
|
ENST00000359218.9:c.77634A>C
(TTN)
|
ENSP00000352154.5:p.Glu25878Asp
|
|
ENST00000460472.6:c.77259A>C
(TTN)
|
ENSP00000434586.1:p.Glu25753Asp
|
|
ENST00000589042.5:c.104454A>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu34818Asp
|
|
ENST00000591111.5:c.99531A>C
(TTN)
|
ENSP00000465570.1:p.Glu33177Asp
|
|
ENST00000615779.4:c.99531A>C
(TTN)
|
ENSP00000483597.1:p.Glu33177Asp
|
|
NM_001256850.1:c.99531A>C
(TTN)
|
NP_001243779.1:p.Glu33177Asp
|
|
NM_001267550.2:c.104454A>C
(TTN)
MANE Select
|
NP_001254479.2:p.Glu34818Asp
|
|
NM_003319.4:c.77259A>C
(TTN)
|
NP_003310.4:p.Glu25753Asp
|
|
NM_133378.4:c.96750A>C
(TTN)
|
NP_596869.4:p.Glu32250Asp
|
|
NM_133432.3:c.77634A>C
(TTN)
|
NP_597676.3:p.Glu25878Asp
|
|
NM_133437.4:c.77835A>C
(TTN)
|
NP_597681.4:p.Glu25945Asp
|
|
NR_038271.1:n.446+8525T>G
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3571T>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.103551A>C
(TTN)
|
XP_011510031.1:p.Glu34517Asp
|
|
XM_011511730.1:c.77445A>C
(TTN)
|
XP_011510032.1:p.Glu25815Asp
|
|
XM_011511731.1:c.77304A>C
(TTN)
|
XP_011510033.1:p.Glu25768Asp
|
|
XM_017004819.1:c.103347A>C
(TTN)
|
XP_016860308.1:p.Glu34449Asp
|
|
XM_017004820.1:c.98745A>C
(TTN)
|
XP_016860309.1:p.Glu32915Asp
|
|
XM_017004821.1:c.98742A>C
(TTN)
|
XP_016860310.1:p.Glu32914Asp
|
|
XM_017004822.1:c.95784A>C
(TTN)
|
XP_016860311.1:p.Glu31928Asp
|
|
XM_017004823.1:c.77400A>C
(TTN)
|
XP_016860312.1:p.Glu25800Asp
|
|
XM_024453094.1:c.98895A>C
(TTN)
|
XP_024308862.1:p.Glu32965Asp
|
|
XM_024453095.1:c.98892A>C
(TTN)
|
XP_024308863.1:p.Glu32964Asp
|
|
XM_024453096.1:c.98325A>C
(TTN)
|
XP_024308864.1:p.Glu32775Asp
|
|
XM_024453097.1:c.95667A>C
(TTN)
|
XP_024308865.1:p.Glu31889Asp
|
|
XM_024453098.1:c.95586A>C
(TTN)
|
XP_024308866.1:p.Glu31862Asp
|
|
XM_024453099.1:c.77349A>C
(TTN)
|
XP_024308867.1:p.Glu25783Asp
|
|
XM_024453100.1:c.67203A>C
(TTN)
|
XP_024308868.1:p.Glu22401Asp
|
|