ENST00000342992.11:c.98733T>A
(TTN)
|
ENSP00000343764.6:p.Ile32911=
|
|
ENST00000342175.11:c.79818T>A
(TTN)
|
ENSP00000340554.6:p.Ile26606=
|
|
ENST00000359218.10:c.79617T>A
(TTN)
|
ENSP00000352154.5:p.Ile26539=
|
|
ENST00000342175.10:c.79818T>A
(TTN)
|
ENSP00000340554.6:p.Ile26606=
|
|
ENST00000342992.10:c.98733T>A
(TTN)
|
ENSP00000343764.6:p.Ile32911=
|
|
ENST00000359218.9:c.79617T>A
(TTN)
|
ENSP00000352154.5:p.Ile26539=
|
|
ENST00000460472.6:c.79242T>A
(TTN)
|
ENSP00000434586.1:p.Ile26414=
|
|
ENST00000589042.5:c.106437T>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ile35479=
|
|
ENST00000591111.5:c.101514T>A
(TTN)
|
ENSP00000465570.1:p.Ile33838=
|
|
ENST00000615779.4:c.101514T>A
(TTN)
|
ENSP00000483597.1:p.Ile33838=
|
|
NM_001256850.1:c.101514T>A
(TTN)
|
NP_001243779.1:p.Ile33838=
|
|
NM_001267550.2:c.106437T>A
(TTN)
MANE Select
|
NP_001254479.2:p.Ile35479=
|
|
NM_003319.4:c.79242T>A
(TTN)
|
NP_003310.4:p.Ile26414=
|
|
NM_133378.4:c.98733T>A
(TTN)
|
NP_596869.4:p.Ile32911=
|
|
NM_133432.3:c.79617T>A
(TTN)
|
NP_597676.3:p.Ile26539=
|
|
NM_133437.4:c.79818T>A
(TTN)
|
NP_597681.4:p.Ile26606=
|
|
NR_038271.1:n.446+6418A>T
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5678A>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.105534T>A
(TTN)
|
XP_011510031.1:p.Ile35178=
|
|
XM_011511730.1:c.79428T>A
(TTN)
|
XP_011510032.1:p.Ile26476=
|
|
XM_011511731.1:c.79287T>A
(TTN)
|
XP_011510033.1:p.Ile26429=
|
|
XM_017004819.1:c.105330T>A
(TTN)
|
XP_016860308.1:p.Ile35110=
|
|
XM_017004820.1:c.100728T>A
(TTN)
|
XP_016860309.1:p.Ile33576=
|
|
XM_017004821.1:c.100725T>A
(TTN)
|
XP_016860310.1:p.Ile33575=
|
|
XM_017004822.1:c.97767T>A
(TTN)
|
XP_016860311.1:p.Ile32589=
|
|
XM_017004823.1:c.79383T>A
(TTN)
|
XP_016860312.1:p.Ile26461=
|
|
XM_024453094.1:c.100878T>A
(TTN)
|
XP_024308862.1:p.Ile33626=
|
|
XM_024453095.1:c.100875T>A
(TTN)
|
XP_024308863.1:p.Ile33625=
|
|
XM_024453096.1:c.100308T>A
(TTN)
|
XP_024308864.1:p.Ile33436=
|
|
XM_024453097.1:c.97650T>A
(TTN)
|
XP_024308865.1:p.Ile32550=
|
|
XM_024453098.1:c.97569T>A
(TTN)
|
XP_024308866.1:p.Ile32523=
|
|
XM_024453099.1:c.79332T>A
(TTN)
|
XP_024308867.1:p.Ile26444=
|
|
XM_024453100.1:c.69186T>A
(TTN)
|
XP_024308868.1:p.Ile23062=
|
|