ENST00000342992.11:c.78598G=
(TTN)
|
ENSP00000343764.6:p.Ala26200=
|
|
ENST00000342175.11:c.59683G=
(TTN)
|
ENSP00000340554.6:p.Ala19895=
|
|
ENST00000359218.10:c.59482G=
(TTN)
|
ENSP00000352154.5:p.Ala19828=
|
|
ENST00000342175.10:c.59683G=
(TTN)
|
ENSP00000340554.6:p.Ala19895=
|
|
ENST00000342992.10:c.78598G=
(TTN)
|
ENSP00000343764.6:p.Ala26200=
|
|
ENST00000359218.9:c.59482G=
(TTN)
|
ENSP00000352154.5:p.Ala19828=
|
|
ENST00000460472.6:c.59107G=
(TTN)
|
ENSP00000434586.1:p.Ala19703=
|
|
ENST00000589042.5:c.86302G=
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ala28768=
|
|
ENST00000591111.5:c.81379G=
(TTN)
|
ENSP00000465570.1:p.Ala27127=
|
|
ENST00000615779.4:c.81379G=
(TTN)
|
ENSP00000483597.1:p.Ala27127=
|
|
NM_001256850.1:c.81379G=
(TTN)
|
NP_001243779.1:p.Ala27127=
|
|
NM_001267550.2:c.86302G=
(TTN)
MANE Select
|
NP_001254479.2:p.Ala28768=
|
|
NM_003319.4:c.59107G=
(TTN)
|
NP_003310.4:p.Ala19703=
|
|
NM_133378.4:c.78598G=
(TTN)
|
NP_596869.4:p.Ala26200=
|
|
NM_133432.3:c.59482G=
(TTN)
|
NP_597676.3:p.Ala19828=
|
|
NM_133437.4:c.59683G=
(TTN)
|
NP_597681.4:p.Ala19895=
|
|
NR_038271.1:n.447-11470C=
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+17469C=
(TTN-AS1)
|
|
|
XM_011511729.1:c.85399G=
(TTN)
|
XP_011510031.1:p.Ala28467=
|
|
XM_011511730.1:c.59293G=
(TTN)
|
XP_011510032.1:p.Ala19765=
|
|
XM_011511731.1:c.59152G=
(TTN)
|
XP_011510033.1:p.Ala19718=
|
|
XM_017004819.1:c.85195G=
(TTN)
|
XP_016860308.1:p.Ala28399=
|
|
XM_017004820.1:c.80593G=
(TTN)
|
XP_016860309.1:p.Ala26865=
|
|
XM_017004821.1:c.80590G=
(TTN)
|
XP_016860310.1:p.Ala26864=
|
|
XM_017004822.1:c.77632G=
(TTN)
|
XP_016860311.1:p.Ala25878=
|
|
XM_017004823.1:c.59248G=
(TTN)
|
XP_016860312.1:p.Ala19750=
|
|
XM_024453094.1:c.80743G=
(TTN)
|
XP_024308862.1:p.Ala26915=
|
|
XM_024453095.1:c.80740G=
(TTN)
|
XP_024308863.1:p.Ala26914=
|
|
XM_024453096.1:c.80173G=
(TTN)
|
XP_024308864.1:p.Ala26725=
|
|
XM_024453097.1:c.77515G=
(TTN)
|
XP_024308865.1:p.Ala25839=
|
|
XM_024453098.1:c.77434G=
(TTN)
|
XP_024308866.1:p.Ala25812=
|
|
XM_024453099.1:c.59197G=
(TTN)
|
XP_024308867.1:p.Ala19733=
|
|
XM_024453100.1:c.49051G=
(TTN)
|
XP_024308868.1:p.Ala16351=
|
|