ENST00000342992.11:c.51357T>G
(TTN)
|
ENSP00000343764.6:p.Pro17119=
|
|
ENST00000342175.11:c.32442T>G
(TTN)
|
ENSP00000340554.6:p.Pro10814=
|
|
ENST00000359218.10:c.32241T>G
(TTN)
|
ENSP00000352154.5:p.Pro10747=
|
|
ENST00000342175.10:c.32442T>G
(TTN)
|
ENSP00000340554.6:p.Pro10814=
|
|
ENST00000342992.10:c.51357T>G
(TTN)
|
ENSP00000343764.6:p.Pro17119=
|
|
ENST00000359218.9:c.32241T>G
(TTN)
|
ENSP00000352154.5:p.Pro10747=
|
|
ENST00000460472.6:c.31866T>G
(TTN)
|
ENSP00000434586.1:p.Pro10622=
|
|
ENST00000589042.5:c.59061T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Pro19687=
|
|
ENST00000591111.5:c.54138T>G
(TTN)
|
ENSP00000465570.1:p.Pro18046=
|
|
ENST00000615779.4:c.54138T>G
(TTN)
|
ENSP00000483597.1:p.Pro18046=
|
|
NM_001256850.1:c.54138T>G
(TTN)
|
NP_001243779.1:p.Pro18046=
|
|
NM_001267550.2:c.59061T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Pro19687=
|
|
NM_003319.4:c.31866T>G
(TTN)
|
NP_003310.4:p.Pro10622=
|
|
NM_133378.4:c.51357T>G
(TTN)
|
NP_596869.4:p.Pro17119=
|
|
NM_133432.3:c.32241T>G
(TTN)
|
NP_597676.3:p.Pro10747=
|
|
NM_133437.4:c.32442T>G
(TTN)
|
NP_597681.4:p.Pro10814=
|
|
NR_038271.1:n.597-4538A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.3364+1744A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.58158T>G
(TTN)
|
XP_011510031.1:p.Pro19386=
|
|
XM_011511730.1:c.32052T>G
(TTN)
|
XP_011510032.1:p.Pro10684=
|
|
XM_011511731.1:c.31911T>G
(TTN)
|
XP_011510033.1:p.Pro10637=
|
|
XM_017004819.1:c.57954T>G
(TTN)
|
XP_016860308.1:p.Pro19318=
|
|
XM_017004820.1:c.53352T>G
(TTN)
|
XP_016860309.1:p.Pro17784=
|
|
XM_017004821.1:c.53349T>G
(TTN)
|
XP_016860310.1:p.Pro17783=
|
|
XM_017004822.1:c.50391T>G
(TTN)
|
XP_016860311.1:p.Pro16797=
|
|
XM_017004823.1:c.32007T>G
(TTN)
|
XP_016860312.1:p.Pro10669=
|
|
XM_024453094.1:c.53502T>G
(TTN)
|
XP_024308862.1:p.Pro17834=
|
|
XM_024453095.1:c.53499T>G
(TTN)
|
XP_024308863.1:p.Pro17833=
|
|
XM_024453096.1:c.52932T>G
(TTN)
|
XP_024308864.1:p.Pro17644=
|
|
XM_024453097.1:c.50274T>G
(TTN)
|
XP_024308865.1:p.Pro16758=
|
|
XM_024453098.1:c.50193T>G
(TTN)
|
XP_024308866.1:p.Pro16731=
|
|
XM_024453099.1:c.31956T>G
(TTN)
|
XP_024308867.1:p.Pro10652=
|
|
XM_024453100.1:c.21810T>G
(TTN)
|
XP_024308868.1:p.Pro7270=
|
|