ENST00000342992.11:c.98429C>A
(TTN)
|
ENSP00000343764.6:p.Ala32810Asp
|
|
ENST00000342175.11:c.79514C>A
(TTN)
|
ENSP00000340554.6:p.Ala26505Asp
|
|
ENST00000359218.10:c.79313C>A
(TTN)
|
ENSP00000352154.5:p.Ala26438Asp
|
|
ENST00000342175.10:c.79514C>A
(TTN)
|
ENSP00000340554.6:p.Ala26505Asp
|
|
ENST00000342992.10:c.98429C>A
(TTN)
|
ENSP00000343764.6:p.Ala32810Asp
|
|
ENST00000359218.9:c.79313C>A
(TTN)
|
ENSP00000352154.5:p.Ala26438Asp
|
|
ENST00000460472.6:c.78938C>A
(TTN)
|
ENSP00000434586.1:p.Ala26313Asp
|
|
ENST00000589042.5:c.106133C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ala35378Asp
|
|
ENST00000591111.5:c.101210C>A
(TTN)
|
ENSP00000465570.1:p.Ala33737Asp
|
|
ENST00000615779.4:c.101210C>A
(TTN)
|
ENSP00000483597.1:p.Ala33737Asp
|
|
NM_001256850.1:c.101210C>A
(TTN)
|
NP_001243779.1:p.Ala33737Asp
|
|
NM_001267550.2:c.106133C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Ala35378Asp
|
|
NM_003319.4:c.78938C>A
(TTN)
|
NP_003310.4:p.Ala26313Asp
|
|
NM_133378.4:c.98429C>A
(TTN)
|
NP_596869.4:p.Ala32810Asp
|
|
NM_133432.3:c.79313C>A
(TTN)
|
NP_597676.3:p.Ala26438Asp
|
|
NM_133437.4:c.79514C>A
(TTN)
|
NP_597681.4:p.Ala26505Asp
|
|
NR_038271.1:n.446+6846G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5250G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.105230C>A
(TTN)
|
XP_011510031.1:p.Ala35077Asp
|
|
XM_011511730.1:c.79124C>A
(TTN)
|
XP_011510032.1:p.Ala26375Asp
|
|
XM_011511731.1:c.78983C>A
(TTN)
|
XP_011510033.1:p.Ala26328Asp
|
|
XM_017004819.1:c.105026C>A
(TTN)
|
XP_016860308.1:p.Ala35009Asp
|
|
XM_017004820.1:c.100424C>A
(TTN)
|
XP_016860309.1:p.Ala33475Asp
|
|
XM_017004821.1:c.100421C>A
(TTN)
|
XP_016860310.1:p.Ala33474Asp
|
|
XM_017004822.1:c.97463C>A
(TTN)
|
XP_016860311.1:p.Ala32488Asp
|
|
XM_017004823.1:c.79079C>A
(TTN)
|
XP_016860312.1:p.Ala26360Asp
|
|
XM_024453094.1:c.100574C>A
(TTN)
|
XP_024308862.1:p.Ala33525Asp
|
|
XM_024453095.1:c.100571C>A
(TTN)
|
XP_024308863.1:p.Ala33524Asp
|
|
XM_024453096.1:c.100004C>A
(TTN)
|
XP_024308864.1:p.Ala33335Asp
|
|
XM_024453097.1:c.97346C>A
(TTN)
|
XP_024308865.1:p.Ala32449Asp
|
|
XM_024453098.1:c.97265C>A
(TTN)
|
XP_024308866.1:p.Ala32422Asp
|
|
XM_024453099.1:c.79028C>A
(TTN)
|
XP_024308867.1:p.Ala26343Asp
|
|
XM_024453100.1:c.68882C>A
(TTN)
|
XP_024308868.1:p.Ala22961Asp
|
|