ENST00000342992.11:c.98730A>G
(TTN)
|
ENSP00000343764.6:p.Glu32910=
|
|
ENST00000342175.11:c.79815A>G
(TTN)
|
ENSP00000340554.6:p.Glu26605=
|
|
ENST00000359218.10:c.79614A>G
(TTN)
|
ENSP00000352154.5:p.Glu26538=
|
|
ENST00000342175.10:c.79815A>G
(TTN)
|
ENSP00000340554.6:p.Glu26605=
|
|
ENST00000342992.10:c.98730A>G
(TTN)
|
ENSP00000343764.6:p.Glu32910=
|
|
ENST00000359218.9:c.79614A>G
(TTN)
|
ENSP00000352154.5:p.Glu26538=
|
|
ENST00000460472.6:c.79239A>G
(TTN)
|
ENSP00000434586.1:p.Glu26413=
|
|
ENST00000589042.5:c.106434A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu35478=
|
|
ENST00000591111.5:c.101511A>G
(TTN)
|
ENSP00000465570.1:p.Glu33837=
|
|
ENST00000615779.4:c.101511A>G
(TTN)
|
ENSP00000483597.1:p.Glu33837=
|
|
NM_001256850.1:c.101511A>G
(TTN)
|
NP_001243779.1:p.Glu33837=
|
|
NM_001267550.2:c.106434A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Glu35478=
|
|
NM_003319.4:c.79239A>G
(TTN)
|
NP_003310.4:p.Glu26413=
|
|
NM_133378.4:c.98730A>G
(TTN)
|
NP_596869.4:p.Glu32910=
|
|
NM_133432.3:c.79614A>G
(TTN)
|
NP_597676.3:p.Glu26538=
|
|
NM_133437.4:c.79815A>G
(TTN)
|
NP_597681.4:p.Glu26605=
|
|
NR_038271.1:n.446+6421T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5675T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.105531A>G
(TTN)
|
XP_011510031.1:p.Glu35177=
|
|
XM_011511730.1:c.79425A>G
(TTN)
|
XP_011510032.1:p.Glu26475=
|
|
XM_011511731.1:c.79284A>G
(TTN)
|
XP_011510033.1:p.Glu26428=
|
|
XM_017004819.1:c.105327A>G
(TTN)
|
XP_016860308.1:p.Glu35109=
|
|
XM_017004820.1:c.100725A>G
(TTN)
|
XP_016860309.1:p.Glu33575=
|
|
XM_017004821.1:c.100722A>G
(TTN)
|
XP_016860310.1:p.Glu33574=
|
|
XM_017004822.1:c.97764A>G
(TTN)
|
XP_016860311.1:p.Glu32588=
|
|
XM_017004823.1:c.79380A>G
(TTN)
|
XP_016860312.1:p.Glu26460=
|
|
XM_024453094.1:c.100875A>G
(TTN)
|
XP_024308862.1:p.Glu33625=
|
|
XM_024453095.1:c.100872A>G
(TTN)
|
XP_024308863.1:p.Glu33624=
|
|
XM_024453096.1:c.100305A>G
(TTN)
|
XP_024308864.1:p.Glu33435=
|
|
XM_024453097.1:c.97647A>G
(TTN)
|
XP_024308865.1:p.Glu32549=
|
|
XM_024453098.1:c.97566A>G
(TTN)
|
XP_024308866.1:p.Glu32522=
|
|
XM_024453099.1:c.79329A>G
(TTN)
|
XP_024308867.1:p.Glu26443=
|
|
XM_024453100.1:c.69183A>G
(TTN)
|
XP_024308868.1:p.Glu23061=
|
|