ENST00000342992.11:c.47349T>G
(TTN)
|
ENSP00000343764.6:p.Ala15783=
|
|
ENST00000342175.11:c.28434T>G
(TTN)
|
ENSP00000340554.6:p.Ala9478=
|
|
ENST00000359218.10:c.28233T>G
(TTN)
|
ENSP00000352154.5:p.Ala9411=
|
|
ENST00000342175.10:c.28434T>G
(TTN)
|
ENSP00000340554.6:p.Ala9478=
|
|
ENST00000342992.10:c.47349T>G
(TTN)
|
ENSP00000343764.6:p.Ala15783=
|
|
ENST00000359218.9:c.28233T>G
(TTN)
|
ENSP00000352154.5:p.Ala9411=
|
|
ENST00000460472.6:c.27858T>G
(TTN)
|
ENSP00000434586.1:p.Ala9286=
|
|
ENST00000589042.5:c.55053T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ala18351=
|
|
ENST00000591111.5:c.50130T>G
(TTN)
|
ENSP00000465570.1:p.Ala16710=
|
|
ENST00000615779.4:c.50130T>G
(TTN)
|
ENSP00000483597.1:p.Ala16710=
|
|
NM_001256850.1:c.50130T>G
(TTN)
|
NP_001243779.1:p.Ala16710=
|
|
NM_001267550.2:c.55053T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Ala18351=
|
|
NM_003319.4:c.27858T>G
(TTN)
|
NP_003310.4:p.Ala9286=
|
|
NM_133378.4:c.47349T>G
(TTN)
|
NP_596869.4:p.Ala15783=
|
|
NM_133432.3:c.28233T>G
(TTN)
|
NP_597676.3:p.Ala9411=
|
|
NM_133437.4:c.28434T>G
(TTN)
|
NP_597681.4:p.Ala9478=
|
|
NR_038271.1:n.682+4668A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.3917+1682A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.54150T>G
(TTN)
|
XP_011510031.1:p.Ala18050=
|
|
XM_011511730.1:c.28044T>G
(TTN)
|
XP_011510032.1:p.Ala9348=
|
|
XM_011511731.1:c.27903T>G
(TTN)
|
XP_011510033.1:p.Ala9301=
|
|
XM_017004819.1:c.53946T>G
(TTN)
|
XP_016860308.1:p.Ala17982=
|
|
XM_017004820.1:c.49344T>G
(TTN)
|
XP_016860309.1:p.Ala16448=
|
|
XM_017004821.1:c.49341T>G
(TTN)
|
XP_016860310.1:p.Ala16447=
|
|
XM_017004822.1:c.46383T>G
(TTN)
|
XP_016860311.1:p.Ala15461=
|
|
XM_017004823.1:c.27999T>G
(TTN)
|
XP_016860312.1:p.Ala9333=
|
|
XM_024453094.1:c.49494T>G
(TTN)
|
XP_024308862.1:p.Ala16498=
|
|
XM_024453095.1:c.49491T>G
(TTN)
|
XP_024308863.1:p.Ala16497=
|
|
XM_024453096.1:c.48924T>G
(TTN)
|
XP_024308864.1:p.Ala16308=
|
|
XM_024453097.1:c.46266T>G
(TTN)
|
XP_024308865.1:p.Ala15422=
|
|
XM_024453098.1:c.46185T>G
(TTN)
|
XP_024308866.1:p.Ala15395=
|
|
XM_024453099.1:c.27948T>G
(TTN)
|
XP_024308867.1:p.Ala9316=
|
|
XM_024453100.1:c.17802T>G
(TTN)
|
XP_024308868.1:p.Ala5934=
|
|