ENST00000342992.11:c.77898T>C
(TTN)
|
ENSP00000343764.6:p.Gly25966=
|
|
ENST00000342175.11:c.58983T>C
(TTN)
|
ENSP00000340554.6:p.Gly19661=
|
|
ENST00000359218.10:c.58782T>C
(TTN)
|
ENSP00000352154.5:p.Gly19594=
|
|
ENST00000342175.10:c.58983T>C
(TTN)
|
ENSP00000340554.6:p.Gly19661=
|
|
ENST00000342992.10:c.77898T>C
(TTN)
|
ENSP00000343764.6:p.Gly25966=
|
|
ENST00000359218.9:c.58782T>C
(TTN)
|
ENSP00000352154.5:p.Gly19594=
|
|
ENST00000460472.6:c.58407T>C
(TTN)
|
ENSP00000434586.1:p.Gly19469=
|
|
ENST00000589042.5:c.85602T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gly28534=
|
|
ENST00000591111.5:c.80679T>C
(TTN)
|
ENSP00000465570.1:p.Gly26893=
|
|
ENST00000615779.4:c.80679T>C
(TTN)
|
ENSP00000483597.1:p.Gly26893=
|
|
NM_001256850.1:c.80679T>C
(TTN)
|
NP_001243779.1:p.Gly26893=
|
|
NM_001267550.2:c.85602T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Gly28534=
|
|
NM_003319.4:c.58407T>C
(TTN)
|
NP_003310.4:p.Gly19469=
|
|
NM_133378.4:c.77898T>C
(TTN)
|
NP_596869.4:p.Gly25966=
|
|
NM_133432.3:c.58782T>C
(TTN)
|
NP_597676.3:p.Gly19594=
|
|
NM_133437.4:c.58983T>C
(TTN)
|
NP_597681.4:p.Gly19661=
|
|
NR_038271.1:n.447-10770A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+18169A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.84699T>C
(TTN)
|
XP_011510031.1:p.Gly28233=
|
|
XM_011511730.1:c.58593T>C
(TTN)
|
XP_011510032.1:p.Gly19531=
|
|
XM_011511731.1:c.58452T>C
(TTN)
|
XP_011510033.1:p.Gly19484=
|
|
XM_017004819.1:c.84495T>C
(TTN)
|
XP_016860308.1:p.Gly28165=
|
|
XM_017004820.1:c.79893T>C
(TTN)
|
XP_016860309.1:p.Gly26631=
|
|
XM_017004821.1:c.79890T>C
(TTN)
|
XP_016860310.1:p.Gly26630=
|
|
XM_017004822.1:c.76932T>C
(TTN)
|
XP_016860311.1:p.Gly25644=
|
|
XM_017004823.1:c.58548T>C
(TTN)
|
XP_016860312.1:p.Gly19516=
|
|
XM_024453094.1:c.80043T>C
(TTN)
|
XP_024308862.1:p.Gly26681=
|
|
XM_024453095.1:c.80040T>C
(TTN)
|
XP_024308863.1:p.Gly26680=
|
|
XM_024453096.1:c.79473T>C
(TTN)
|
XP_024308864.1:p.Gly26491=
|
|
XM_024453097.1:c.76815T>C
(TTN)
|
XP_024308865.1:p.Gly25605=
|
|
XM_024453098.1:c.76734T>C
(TTN)
|
XP_024308866.1:p.Gly25578=
|
|
XM_024453099.1:c.58497T>C
(TTN)
|
XP_024308867.1:p.Gly19499=
|
|
XM_024453100.1:c.48351T>C
(TTN)
|
XP_024308868.1:p.Gly16117=
|
|