ENST00000342992.11:c.100268T>C
(TTN)
|
ENSP00000343764.6:p.Ile33423Thr
|
|
ENST00000342175.11:c.81353T>C
(TTN)
|
ENSP00000340554.6:p.Ile27118Thr
|
|
ENST00000359218.10:c.81152T>C
(TTN)
|
ENSP00000352154.5:p.Ile27051Thr
|
|
ENST00000342175.10:c.81353T>C
(TTN)
|
ENSP00000340554.6:p.Ile27118Thr
|
|
ENST00000342992.10:c.100268T>C
(TTN)
|
ENSP00000343764.6:p.Ile33423Thr
|
|
ENST00000359218.9:c.81152T>C
(TTN)
|
ENSP00000352154.5:p.Ile27051Thr
|
|
ENST00000460472.6:c.80777T>C
(TTN)
|
ENSP00000434586.1:p.Ile26926Thr
|
|
ENST00000589042.5:c.107972T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ile35991Thr
|
|
ENST00000591111.5:c.103049T>C
(TTN)
|
ENSP00000465570.1:p.Ile34350Thr
|
|
ENST00000615779.4:c.103049T>C
(TTN)
|
ENSP00000483597.1:p.Ile34350Thr
|
|
NM_001256850.1:c.103049T>C
(TTN)
|
NP_001243779.1:p.Ile34350Thr
|
|
NM_001267550.2:c.107972T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Ile35991Thr
|
|
NM_003319.4:c.80777T>C
(TTN)
|
NP_003310.4:p.Ile26926Thr
|
|
NM_133378.4:c.100268T>C
(TTN)
|
NP_596869.4:p.Ile33423Thr
|
|
NM_133432.3:c.81152T>C
(TTN)
|
NP_597676.3:p.Ile27051Thr
|
|
NM_133437.4:c.81353T>C
(TTN)
|
NP_597681.4:p.Ile27118Thr
|
|
NR_038271.1:n.446+3380A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.219+3380A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.107069T>C
(TTN)
|
XP_011510031.1:p.Ile35690Thr
|
|
XM_011511730.1:c.80963T>C
(TTN)
|
XP_011510032.1:p.Ile26988Thr
|
|
XM_011511731.1:c.80822T>C
(TTN)
|
XP_011510033.1:p.Ile26941Thr
|
|
XM_017004819.1:c.106865T>C
(TTN)
|
XP_016860308.1:p.Ile35622Thr
|
|
XM_017004820.1:c.102263T>C
(TTN)
|
XP_016860309.1:p.Ile34088Thr
|
|
XM_017004821.1:c.102260T>C
(TTN)
|
XP_016860310.1:p.Ile34087Thr
|
|
XM_017004822.1:c.99302T>C
(TTN)
|
XP_016860311.1:p.Ile33101Thr
|
|
XM_017004823.1:c.80918T>C
(TTN)
|
XP_016860312.1:p.Ile26973Thr
|
|
XM_024453094.1:c.102413T>C
(TTN)
|
XP_024308862.1:p.Ile34138Thr
|
|
XM_024453095.1:c.102410T>C
(TTN)
|
XP_024308863.1:p.Ile34137Thr
|
|
XM_024453096.1:c.101843T>C
(TTN)
|
XP_024308864.1:p.Ile33948Thr
|
|
XM_024453097.1:c.99185T>C
(TTN)
|
XP_024308865.1:p.Ile33062Thr
|
|
XM_024453098.1:c.99104T>C
(TTN)
|
XP_024308866.1:p.Ile33035Thr
|
|
XM_024453099.1:c.80867T>C
(TTN)
|
XP_024308867.1:p.Ile26956Thr
|
|
XM_024453100.1:c.70721T>C
(TTN)
|
XP_024308868.1:p.Ile23574Thr
|
|