ENST00000342992.11:c.84255C>G
(TTN)
|
ENSP00000343764.6:p.Thr28085=
|
|
ENST00000342175.11:c.65340C>G
(TTN)
|
ENSP00000340554.6:p.Thr21780=
|
|
ENST00000359218.10:c.65139C>G
(TTN)
|
ENSP00000352154.5:p.Thr21713=
|
|
ENST00000342175.10:c.65340C>G
(TTN)
|
ENSP00000340554.6:p.Thr21780=
|
|
ENST00000342992.10:c.84255C>G
(TTN)
|
ENSP00000343764.6:p.Thr28085=
|
|
ENST00000359218.9:c.65139C>G
(TTN)
|
ENSP00000352154.5:p.Thr21713=
|
|
ENST00000460472.6:c.64764C>G
(TTN)
|
ENSP00000434586.1:p.Thr21588=
|
|
ENST00000589042.5:c.91959C>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr30653=
|
|
ENST00000591111.5:c.87036C>G
(TTN)
|
ENSP00000465570.1:p.Thr29012=
|
|
ENST00000615779.4:c.87036C>G
(TTN)
|
ENSP00000483597.1:p.Thr29012=
|
|
NM_001256850.1:c.87036C>G
(TTN)
|
NP_001243779.1:p.Thr29012=
|
|
NM_001267550.2:c.91959C>G
(TTN)
MANE Select
|
NP_001254479.2:p.Thr30653=
|
|
NM_003319.4:c.64764C>G
(TTN)
|
NP_003310.4:p.Thr21588=
|
|
NM_133378.4:c.84255C>G
(TTN)
|
NP_596869.4:p.Thr28085=
|
|
NM_133432.3:c.65139C>G
(TTN)
|
NP_597676.3:p.Thr21713=
|
|
NM_133437.4:c.65340C>G
(TTN)
|
NP_597681.4:p.Thr21780=
|
|
NR_038271.1:n.447-21537G>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+7402G>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.91056C>G
(TTN)
|
XP_011510031.1:p.Thr30352=
|
|
XM_011511730.1:c.64950C>G
(TTN)
|
XP_011510032.1:p.Thr21650=
|
|
XM_011511731.1:c.64809C>G
(TTN)
|
XP_011510033.1:p.Thr21603=
|
|
XM_017004819.1:c.90852C>G
(TTN)
|
XP_016860308.1:p.Thr30284=
|
|
XM_017004820.1:c.86250C>G
(TTN)
|
XP_016860309.1:p.Thr28750=
|
|
XM_017004821.1:c.86247C>G
(TTN)
|
XP_016860310.1:p.Thr28749=
|
|
XM_017004822.1:c.83289C>G
(TTN)
|
XP_016860311.1:p.Thr27763=
|
|
XM_017004823.1:c.64905C>G
(TTN)
|
XP_016860312.1:p.Thr21635=
|
|
XM_024453094.1:c.86400C>G
(TTN)
|
XP_024308862.1:p.Thr28800=
|
|
XM_024453095.1:c.86397C>G
(TTN)
|
XP_024308863.1:p.Thr28799=
|
|
XM_024453096.1:c.85830C>G
(TTN)
|
XP_024308864.1:p.Thr28610=
|
|
XM_024453097.1:c.83172C>G
(TTN)
|
XP_024308865.1:p.Thr27724=
|
|
XM_024453098.1:c.83091C>G
(TTN)
|
XP_024308866.1:p.Thr27697=
|
|
XM_024453099.1:c.64854C>G
(TTN)
|
XP_024308867.1:p.Thr21618=
|
|
XM_024453100.1:c.54708C>G
(TTN)
|
XP_024308868.1:p.Thr18236=
|
|