ENST00000342992.11:c.67985T>G
(TTN)
|
ENSP00000343764.6:p.Leu22662Arg
|
|
ENST00000342175.11:c.49070T>G
(TTN)
|
ENSP00000340554.6:p.Leu16357Arg
|
|
ENST00000359218.10:c.48869T>G
(TTN)
|
ENSP00000352154.5:p.Leu16290Arg
|
|
ENST00000342175.10:c.49070T>G
(TTN)
|
ENSP00000340554.6:p.Leu16357Arg
|
|
ENST00000342992.10:c.67985T>G
(TTN)
|
ENSP00000343764.6:p.Leu22662Arg
|
|
ENST00000359218.9:c.48869T>G
(TTN)
|
ENSP00000352154.5:p.Leu16290Arg
|
|
ENST00000460472.6:c.48494T>G
(TTN)
|
ENSP00000434586.1:p.Leu16165Arg
|
|
ENST00000589042.5:c.75689T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu25230Arg
|
|
ENST00000591111.5:c.70766T>G
(TTN)
|
ENSP00000465570.1:p.Leu23589Arg
|
|
ENST00000615779.4:c.70766T>G
(TTN)
|
ENSP00000483597.1:p.Leu23589Arg
|
|
NM_001256850.1:c.70766T>G
(TTN)
|
NP_001243779.1:p.Leu23589Arg
|
|
NM_001267550.2:c.75689T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Leu25230Arg
|
|
NM_003319.4:c.48494T>G
(TTN)
|
NP_003310.4:p.Leu16165Arg
|
|
NM_133378.4:c.67985T>G
(TTN)
|
NP_596869.4:p.Leu22662Arg
|
|
NM_133432.3:c.48869T>G
(TTN)
|
NP_597676.3:p.Leu16290Arg
|
|
NM_133437.4:c.49070T>G
(TTN)
|
NP_597681.4:p.Leu16357Arg
|
|
NR_038271.1:n.447-857A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-12129A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.74786T>G
(TTN)
|
XP_011510031.1:p.Leu24929Arg
|
|
XM_011511730.1:c.48680T>G
(TTN)
|
XP_011510032.1:p.Leu16227Arg
|
|
XM_011511731.1:c.48539T>G
(TTN)
|
XP_011510033.1:p.Leu16180Arg
|
|
XM_017004819.1:c.74582T>G
(TTN)
|
XP_016860308.1:p.Leu24861Arg
|
|
XM_017004820.1:c.69980T>G
(TTN)
|
XP_016860309.1:p.Leu23327Arg
|
|
XM_017004821.1:c.69977T>G
(TTN)
|
XP_016860310.1:p.Leu23326Arg
|
|
XM_017004822.1:c.67019T>G
(TTN)
|
XP_016860311.1:p.Leu22340Arg
|
|
XM_017004823.1:c.48635T>G
(TTN)
|
XP_016860312.1:p.Leu16212Arg
|
|
XM_024453094.1:c.70130T>G
(TTN)
|
XP_024308862.1:p.Leu23377Arg
|
|
XM_024453095.1:c.70127T>G
(TTN)
|
XP_024308863.1:p.Leu23376Arg
|
|
XM_024453096.1:c.69560T>G
(TTN)
|
XP_024308864.1:p.Leu23187Arg
|
|
XM_024453097.1:c.66902T>G
(TTN)
|
XP_024308865.1:p.Leu22301Arg
|
|
XM_024453098.1:c.66821T>G
(TTN)
|
XP_024308866.1:p.Leu22274Arg
|
|
XM_024453099.1:c.48584T>G
(TTN)
|
XP_024308867.1:p.Leu16195Arg
|
|
XM_024453100.1:c.38438T>G
(TTN)
|
XP_024308868.1:p.Leu12813Arg
|
|