ENST00000342992.11:c.87831C>T
(TTN)
|
ENSP00000343764.6:p.Asp29277=
|
|
ENST00000342175.11:c.68916C>T
(TTN)
|
ENSP00000340554.6:p.Asp22972=
|
|
ENST00000359218.10:c.68715C>T
(TTN)
|
ENSP00000352154.5:p.Asp22905=
|
|
ENST00000342175.10:c.68916C>T
(TTN)
|
ENSP00000340554.6:p.Asp22972=
|
|
ENST00000342992.10:c.87831C>T
(TTN)
|
ENSP00000343764.6:p.Asp29277=
|
|
ENST00000359218.9:c.68715C>T
(TTN)
|
ENSP00000352154.5:p.Asp22905=
|
|
ENST00000460472.6:c.68340C>T
(TTN)
|
ENSP00000434586.1:p.Asp22780=
|
|
ENST00000589042.5:c.95535C>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp31845=
|
|
ENST00000591111.5:c.90612C>T
(TTN)
|
ENSP00000465570.1:p.Asp30204=
|
|
ENST00000615779.4:c.90612C>T
(TTN)
|
ENSP00000483597.1:p.Asp30204=
|
|
NM_001256850.1:c.90612C>T
(TTN)
|
NP_001243779.1:p.Asp30204=
|
|
NM_001267550.2:c.95535C>T
(TTN)
MANE Select
|
NP_001254479.2:p.Asp31845=
|
|
NM_003319.4:c.68340C>T
(TTN)
|
NP_003310.4:p.Asp22780=
|
|
NM_133378.4:c.87831C>T
(TTN)
|
NP_596869.4:p.Asp29277=
|
|
NM_133432.3:c.68715C>T
(TTN)
|
NP_597676.3:p.Asp22905=
|
|
NM_133437.4:c.68916C>T
(TTN)
|
NP_597681.4:p.Asp22972=
|
|
NR_038271.1:n.446+21939G>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+3214G>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.94632C>T
(TTN)
|
XP_011510031.1:p.Asp31544=
|
|
XM_011511730.1:c.68526C>T
(TTN)
|
XP_011510032.1:p.Asp22842=
|
|
XM_011511731.1:c.68385C>T
(TTN)
|
XP_011510033.1:p.Asp22795=
|
|
XM_017004819.1:c.94428C>T
(TTN)
|
XP_016860308.1:p.Asp31476=
|
|
XM_017004820.1:c.89826C>T
(TTN)
|
XP_016860309.1:p.Asp29942=
|
|
XM_017004821.1:c.89823C>T
(TTN)
|
XP_016860310.1:p.Asp29941=
|
|
XM_017004822.1:c.86865C>T
(TTN)
|
XP_016860311.1:p.Asp28955=
|
|
XM_017004823.1:c.68481C>T
(TTN)
|
XP_016860312.1:p.Asp22827=
|
|
XM_024453094.1:c.89976C>T
(TTN)
|
XP_024308862.1:p.Asp29992=
|
|
XM_024453095.1:c.89973C>T
(TTN)
|
XP_024308863.1:p.Asp29991=
|
|
XM_024453096.1:c.89406C>T
(TTN)
|
XP_024308864.1:p.Asp29802=
|
|
XM_024453097.1:c.86748C>T
(TTN)
|
XP_024308865.1:p.Asp28916=
|
|
XM_024453098.1:c.86667C>T
(TTN)
|
XP_024308866.1:p.Asp28889=
|
|
XM_024453099.1:c.68430C>T
(TTN)
|
XP_024308867.1:p.Asp22810=
|
|
XM_024453100.1:c.58284C>T
(TTN)
|
XP_024308868.1:p.Asp19428=
|
|