ENST00000342992.11:c.69003C>A
(TTN)
|
ENSP00000343764.6:p.Asp23001Glu
|
|
ENST00000342175.11:c.50088C>A
(TTN)
|
ENSP00000340554.6:p.Asp16696Glu
|
|
ENST00000359218.10:c.49887C>A
(TTN)
|
ENSP00000352154.5:p.Asp16629Glu
|
|
ENST00000342175.10:c.50088C>A
(TTN)
|
ENSP00000340554.6:p.Asp16696Glu
|
|
ENST00000342992.10:c.69003C>A
(TTN)
|
ENSP00000343764.6:p.Asp23001Glu
|
|
ENST00000359218.9:c.49887C>A
(TTN)
|
ENSP00000352154.5:p.Asp16629Glu
|
|
ENST00000460472.6:c.49512C>A
(TTN)
|
ENSP00000434586.1:p.Asp16504Glu
|
|
ENST00000589042.5:c.76707C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp25569Glu
|
|
ENST00000591111.5:c.71784C>A
(TTN)
|
ENSP00000465570.1:p.Asp23928Glu
|
|
ENST00000615779.4:c.71784C>A
(TTN)
|
ENSP00000483597.1:p.Asp23928Glu
|
|
NM_001256850.1:c.71784C>A
(TTN)
|
NP_001243779.1:p.Asp23928Glu
|
|
NM_001267550.2:c.76707C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Asp25569Glu
|
|
NM_003319.4:c.49512C>A
(TTN)
|
NP_003310.4:p.Asp16504Glu
|
|
NM_133378.4:c.69003C>A
(TTN)
|
NP_596869.4:p.Asp23001Glu
|
|
NM_133432.3:c.49887C>A
(TTN)
|
NP_597676.3:p.Asp16629Glu
|
|
NM_133437.4:c.50088C>A
(TTN)
|
NP_597681.4:p.Asp16696Glu
|
|
NR_038271.1:n.447-1875G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-13147G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.75804C>A
(TTN)
|
XP_011510031.1:p.Asp25268Glu
|
|
XM_011511730.1:c.49698C>A
(TTN)
|
XP_011510032.1:p.Asp16566Glu
|
|
XM_011511731.1:c.49557C>A
(TTN)
|
XP_011510033.1:p.Asp16519Glu
|
|
XM_017004819.1:c.75600C>A
(TTN)
|
XP_016860308.1:p.Asp25200Glu
|
|
XM_017004820.1:c.70998C>A
(TTN)
|
XP_016860309.1:p.Asp23666Glu
|
|
XM_017004821.1:c.70995C>A
(TTN)
|
XP_016860310.1:p.Asp23665Glu
|
|
XM_017004822.1:c.68037C>A
(TTN)
|
XP_016860311.1:p.Asp22679Glu
|
|
XM_017004823.1:c.49653C>A
(TTN)
|
XP_016860312.1:p.Asp16551Glu
|
|
XM_024453094.1:c.71148C>A
(TTN)
|
XP_024308862.1:p.Asp23716Glu
|
|
XM_024453095.1:c.71145C>A
(TTN)
|
XP_024308863.1:p.Asp23715Glu
|
|
XM_024453096.1:c.70578C>A
(TTN)
|
XP_024308864.1:p.Asp23526Glu
|
|
XM_024453097.1:c.67920C>A
(TTN)
|
XP_024308865.1:p.Asp22640Glu
|
|
XM_024453098.1:c.67839C>A
(TTN)
|
XP_024308866.1:p.Asp22613Glu
|
|
XM_024453099.1:c.49602C>A
(TTN)
|
XP_024308867.1:p.Asp16534Glu
|
|
XM_024453100.1:c.39456C>A
(TTN)
|
XP_024308868.1:p.Asp13152Glu
|
|