ENST00000342992.11:c.100153C>A
(TTN)
|
ENSP00000343764.6:p.Leu33385Met
|
|
ENST00000342175.11:c.81238C>A
(TTN)
|
ENSP00000340554.6:p.Leu27080Met
|
|
ENST00000359218.10:c.81037C>A
(TTN)
|
ENSP00000352154.5:p.Leu27013Met
|
|
ENST00000342175.10:c.81238C>A
(TTN)
|
ENSP00000340554.6:p.Leu27080Met
|
|
ENST00000342992.10:c.100153C>A
(TTN)
|
ENSP00000343764.6:p.Leu33385Met
|
|
ENST00000359218.9:c.81037C>A
(TTN)
|
ENSP00000352154.5:p.Leu27013Met
|
|
ENST00000460472.6:c.80662C>A
(TTN)
|
ENSP00000434586.1:p.Leu26888Met
|
|
ENST00000589042.5:c.107857C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu35953Met
|
|
ENST00000591111.5:c.102934C>A
(TTN)
|
ENSP00000465570.1:p.Leu34312Met
|
|
ENST00000615779.4:c.102934C>A
(TTN)
|
ENSP00000483597.1:p.Leu34312Met
|
|
NM_001256850.1:c.102934C>A
(TTN)
|
NP_001243779.1:p.Leu34312Met
|
|
NM_001267550.2:c.107857C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Leu35953Met
|
|
NM_003319.4:c.80662C>A
(TTN)
|
NP_003310.4:p.Leu26888Met
|
|
NM_133378.4:c.100153C>A
(TTN)
|
NP_596869.4:p.Leu33385Met
|
|
NM_133432.3:c.81037C>A
(TTN)
|
NP_597676.3:p.Leu27013Met
|
|
NM_133437.4:c.81238C>A
(TTN)
|
NP_597681.4:p.Leu27080Met
|
|
NR_038271.1:n.446+3495G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.219+3495G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.106954C>A
(TTN)
|
XP_011510031.1:p.Leu35652Met
|
|
XM_011511730.1:c.80848C>A
(TTN)
|
XP_011510032.1:p.Leu26950Met
|
|
XM_011511731.1:c.80707C>A
(TTN)
|
XP_011510033.1:p.Leu26903Met
|
|
XM_017004819.1:c.106750C>A
(TTN)
|
XP_016860308.1:p.Leu35584Met
|
|
XM_017004820.1:c.102148C>A
(TTN)
|
XP_016860309.1:p.Leu34050Met
|
|
XM_017004821.1:c.102145C>A
(TTN)
|
XP_016860310.1:p.Leu34049Met
|
|
XM_017004822.1:c.99187C>A
(TTN)
|
XP_016860311.1:p.Leu33063Met
|
|
XM_017004823.1:c.80803C>A
(TTN)
|
XP_016860312.1:p.Leu26935Met
|
|
XM_024453094.1:c.102298C>A
(TTN)
|
XP_024308862.1:p.Leu34100Met
|
|
XM_024453095.1:c.102295C>A
(TTN)
|
XP_024308863.1:p.Leu34099Met
|
|
XM_024453096.1:c.101728C>A
(TTN)
|
XP_024308864.1:p.Leu33910Met
|
|
XM_024453097.1:c.99070C>A
(TTN)
|
XP_024308865.1:p.Leu33024Met
|
|
XM_024453098.1:c.98989C>A
(TTN)
|
XP_024308866.1:p.Leu32997Met
|
|
XM_024453099.1:c.80752C>A
(TTN)
|
XP_024308867.1:p.Leu26918Met
|
|
XM_024453100.1:c.70606C>A
(TTN)
|
XP_024308868.1:p.Leu23536Met
|
|