ENST00000342992.11:c.98287C>G
(TTN)
|
ENSP00000343764.6:p.His32763Asp
|
|
ENST00000342175.11:c.79372C>G
(TTN)
|
ENSP00000340554.6:p.His26458Asp
|
|
ENST00000359218.10:c.79171C>G
(TTN)
|
ENSP00000352154.5:p.His26391Asp
|
|
ENST00000342175.10:c.79372C>G
(TTN)
|
ENSP00000340554.6:p.His26458Asp
|
|
ENST00000342992.10:c.98287C>G
(TTN)
|
ENSP00000343764.6:p.His32763Asp
|
|
ENST00000359218.9:c.79171C>G
(TTN)
|
ENSP00000352154.5:p.His26391Asp
|
|
ENST00000460472.6:c.78796C>G
(TTN)
|
ENSP00000434586.1:p.His26266Asp
|
|
ENST00000589042.5:c.105991C>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.His35331Asp
|
|
ENST00000591111.5:c.101068C>G
(TTN)
|
ENSP00000465570.1:p.His33690Asp
|
|
ENST00000615779.4:c.101068C>G
(TTN)
|
ENSP00000483597.1:p.His33690Asp
|
|
NM_001256850.1:c.101068C>G
(TTN)
|
NP_001243779.1:p.His33690Asp
|
|
NM_001267550.2:c.105991C>G
(TTN)
MANE Select
|
NP_001254479.2:p.His35331Asp
|
|
NM_003319.4:c.78796C>G
(TTN)
|
NP_003310.4:p.His26266Asp
|
|
NM_133378.4:c.98287C>G
(TTN)
|
NP_596869.4:p.His32763Asp
|
|
NM_133432.3:c.79171C>G
(TTN)
|
NP_597676.3:p.His26391Asp
|
|
NM_133437.4:c.79372C>G
(TTN)
|
NP_597681.4:p.His26458Asp
|
|
NR_038271.1:n.446+6988G>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5108G>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.105088C>G
(TTN)
|
XP_011510031.1:p.His35030Asp
|
|
XM_011511730.1:c.78982C>G
(TTN)
|
XP_011510032.1:p.His26328Asp
|
|
XM_011511731.1:c.78841C>G
(TTN)
|
XP_011510033.1:p.His26281Asp
|
|
XM_017004819.1:c.104884C>G
(TTN)
|
XP_016860308.1:p.His34962Asp
|
|
XM_017004820.1:c.100282C>G
(TTN)
|
XP_016860309.1:p.His33428Asp
|
|
XM_017004821.1:c.100279C>G
(TTN)
|
XP_016860310.1:p.His33427Asp
|
|
XM_017004822.1:c.97321C>G
(TTN)
|
XP_016860311.1:p.His32441Asp
|
|
XM_017004823.1:c.78937C>G
(TTN)
|
XP_016860312.1:p.His26313Asp
|
|
XM_024453094.1:c.100432C>G
(TTN)
|
XP_024308862.1:p.His33478Asp
|
|
XM_024453095.1:c.100429C>G
(TTN)
|
XP_024308863.1:p.His33477Asp
|
|
XM_024453096.1:c.99862C>G
(TTN)
|
XP_024308864.1:p.His33288Asp
|
|
XM_024453097.1:c.97204C>G
(TTN)
|
XP_024308865.1:p.His32402Asp
|
|
XM_024453098.1:c.97123C>G
(TTN)
|
XP_024308866.1:p.His32375Asp
|
|
XM_024453099.1:c.78886C>G
(TTN)
|
XP_024308867.1:p.His26296Asp
|
|
XM_024453100.1:c.68740C>G
(TTN)
|
XP_024308868.1:p.His22914Asp
|
|