ENST00000342992.11:c.98672C>A
(TTN)
|
ENSP00000343764.6:p.Ala32891Asp
|
|
ENST00000342175.11:c.79757C>A
(TTN)
|
ENSP00000340554.6:p.Ala26586Asp
|
|
ENST00000359218.10:c.79556C>A
(TTN)
|
ENSP00000352154.5:p.Ala26519Asp
|
|
ENST00000342175.10:c.79757C>A
(TTN)
|
ENSP00000340554.6:p.Ala26586Asp
|
|
ENST00000342992.10:c.98672C>A
(TTN)
|
ENSP00000343764.6:p.Ala32891Asp
|
|
ENST00000359218.9:c.79556C>A
(TTN)
|
ENSP00000352154.5:p.Ala26519Asp
|
|
ENST00000460472.6:c.79181C>A
(TTN)
|
ENSP00000434586.1:p.Ala26394Asp
|
|
ENST00000589042.5:c.106376C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ala35459Asp
|
|
ENST00000591111.5:c.101453C>A
(TTN)
|
ENSP00000465570.1:p.Ala33818Asp
|
|
ENST00000615779.4:c.101453C>A
(TTN)
|
ENSP00000483597.1:p.Ala33818Asp
|
|
NM_001256850.1:c.101453C>A
(TTN)
|
NP_001243779.1:p.Ala33818Asp
|
|
NM_001267550.2:c.106376C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Ala35459Asp
|
|
NM_003319.4:c.79181C>A
(TTN)
|
NP_003310.4:p.Ala26394Asp
|
|
NM_133378.4:c.98672C>A
(TTN)
|
NP_596869.4:p.Ala32891Asp
|
|
NM_133432.3:c.79556C>A
(TTN)
|
NP_597676.3:p.Ala26519Asp
|
|
NM_133437.4:c.79757C>A
(TTN)
|
NP_597681.4:p.Ala26586Asp
|
|
NR_038271.1:n.446+6479G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5617G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.105473C>A
(TTN)
|
XP_011510031.1:p.Ala35158Asp
|
|
XM_011511730.1:c.79367C>A
(TTN)
|
XP_011510032.1:p.Ala26456Asp
|
|
XM_011511731.1:c.79226C>A
(TTN)
|
XP_011510033.1:p.Ala26409Asp
|
|
XM_017004819.1:c.105269C>A
(TTN)
|
XP_016860308.1:p.Ala35090Asp
|
|
XM_017004820.1:c.100667C>A
(TTN)
|
XP_016860309.1:p.Ala33556Asp
|
|
XM_017004821.1:c.100664C>A
(TTN)
|
XP_016860310.1:p.Ala33555Asp
|
|
XM_017004822.1:c.97706C>A
(TTN)
|
XP_016860311.1:p.Ala32569Asp
|
|
XM_017004823.1:c.79322C>A
(TTN)
|
XP_016860312.1:p.Ala26441Asp
|
|
XM_024453094.1:c.100817C>A
(TTN)
|
XP_024308862.1:p.Ala33606Asp
|
|
XM_024453095.1:c.100814C>A
(TTN)
|
XP_024308863.1:p.Ala33605Asp
|
|
XM_024453096.1:c.100247C>A
(TTN)
|
XP_024308864.1:p.Ala33416Asp
|
|
XM_024453097.1:c.97589C>A
(TTN)
|
XP_024308865.1:p.Ala32530Asp
|
|
XM_024453098.1:c.97508C>A
(TTN)
|
XP_024308866.1:p.Ala32503Asp
|
|
XM_024453099.1:c.79271C>A
(TTN)
|
XP_024308867.1:p.Ala26424Asp
|
|
XM_024453100.1:c.69125C>A
(TTN)
|
XP_024308868.1:p.Ala23042Asp
|
|