|
ENST00000342992.11:c.94275C>T
(TTN)
|
ENSP00000343764.6:p.Ser31425=
|
|
|
ENST00000342175.11:c.75360C>T
(TTN)
|
ENSP00000340554.6:p.Ser25120=
|
|
|
ENST00000359218.10:c.75159C>T
(TTN)
|
ENSP00000352154.5:p.Ser25053=
|
|
|
ENST00000342175.10:c.75360C>T
(TTN)
|
ENSP00000340554.6:p.Ser25120=
|
|
|
ENST00000342992.10:c.94275C>T
(TTN)
|
ENSP00000343764.6:p.Ser31425=
|
|
|
ENST00000359218.9:c.75159C>T
(TTN)
|
ENSP00000352154.5:p.Ser25053=
|
|
|
ENST00000460472.6:c.74784C>T
(TTN)
|
ENSP00000434586.1:p.Ser24928=
|
|
|
ENST00000589042.5:c.101979C>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ser33993=
|
|
|
ENST00000591111.5:c.97056C>T
(TTN)
|
ENSP00000465570.1:p.Ser32352=
|
|
|
ENST00000615779.4:c.97056C>T
(TTN)
|
ENSP00000483597.1:p.Ser32352=
|
|
|
NM_001256850.1:c.97056C>T
(TTN)
|
NP_001243779.1:p.Ser32352=
|
|
|
NM_001267550.2:c.101979C>T
(TTN)
MANE Select
|
NP_001254479.2:p.Ser33993=
|
|
|
NM_003319.4:c.74784C>T
(TTN)
|
NP_003310.4:p.Ser24928=
|
|
|
NM_133378.4:c.94275C>T
(TTN)
|
NP_596869.4:p.Ser31425=
|
|
|
NM_133432.3:c.75159C>T
(TTN)
|
NP_597676.3:p.Ser25053=
|
|
|
NM_133437.4:c.75360C>T
(TTN)
|
NP_597681.4:p.Ser25120=
|
|
|
NR_038271.1:n.446+11000G>A
(TTN-AS1)
|
|
|
|
NR_038272.1:n.220-1096G>A
(TTN-AS1)
|
|
|
|
XM_011511729.1:c.101076C>T
(TTN)
|
XP_011510031.1:p.Ser33692=
|
|
|
XM_011511730.1:c.74970C>T
(TTN)
|
XP_011510032.1:p.Ser24990=
|
|
|
XM_011511731.1:c.74829C>T
(TTN)
|
XP_011510033.1:p.Ser24943=
|
|
|
XM_017004819.1:c.100872C>T
(TTN)
|
XP_016860308.1:p.Ser33624=
|
|
|
XM_017004820.1:c.96270C>T
(TTN)
|
XP_016860309.1:p.Ser32090=
|
|
|
XM_017004821.1:c.96267C>T
(TTN)
|
XP_016860310.1:p.Ser32089=
|
|
|
XM_017004822.1:c.93309C>T
(TTN)
|
XP_016860311.1:p.Ser31103=
|
|
|
XM_017004823.1:c.74925C>T
(TTN)
|
XP_016860312.1:p.Ser24975=
|
|
|
XM_024453094.1:c.96420C>T
(TTN)
|
XP_024308862.1:p.Ser32140=
|
|
|
XM_024453095.1:c.96417C>T
(TTN)
|
XP_024308863.1:p.Ser32139=
|
|
|
XM_024453096.1:c.95850C>T
(TTN)
|
XP_024308864.1:p.Ser31950=
|
|
|
XM_024453097.1:c.93192C>T
(TTN)
|
XP_024308865.1:p.Ser31064=
|
|
|
XM_024453098.1:c.93111C>T
(TTN)
|
XP_024308866.1:p.Ser31037=
|
|
|
XM_024453099.1:c.74874C>T
(TTN)
|
XP_024308867.1:p.Ser24958=
|
|
|
XM_024453100.1:c.64728C>T
(TTN)
|
XP_024308868.1:p.Ser21576=
|
|
