ENST00000342992.11:c.67868G>C
(TTN)
|
ENSP00000343764.6:p.Gly22623Ala
|
|
ENST00000342175.11:c.48953G>C
(TTN)
|
ENSP00000340554.6:p.Gly16318Ala
|
|
ENST00000359218.10:c.48752G>C
(TTN)
|
ENSP00000352154.5:p.Gly16251Ala
|
|
ENST00000342175.10:c.48953G>C
(TTN)
|
ENSP00000340554.6:p.Gly16318Ala
|
|
ENST00000342992.10:c.67868G>C
(TTN)
|
ENSP00000343764.6:p.Gly22623Ala
|
|
ENST00000359218.9:c.48752G>C
(TTN)
|
ENSP00000352154.5:p.Gly16251Ala
|
|
ENST00000460472.6:c.48377G>C
(TTN)
|
ENSP00000434586.1:p.Gly16126Ala
|
|
ENST00000589042.5:c.75572G>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gly25191Ala
|
|
ENST00000591111.5:c.70649G>C
(TTN)
|
ENSP00000465570.1:p.Gly23550Ala
|
|
ENST00000615779.4:c.70649G>C
(TTN)
|
ENSP00000483597.1:p.Gly23550Ala
|
|
NM_001256850.1:c.70649G>C
(TTN)
|
NP_001243779.1:p.Gly23550Ala
|
|
NM_001267550.2:c.75572G>C
(TTN)
MANE Select
|
NP_001254479.2:p.Gly25191Ala
|
|
NM_003319.4:c.48377G>C
(TTN)
|
NP_003310.4:p.Gly16126Ala
|
|
NM_133378.4:c.67868G>C
(TTN)
|
NP_596869.4:p.Gly22623Ala
|
|
NM_133432.3:c.48752G>C
(TTN)
|
NP_597676.3:p.Gly16251Ala
|
|
NM_133437.4:c.48953G>C
(TTN)
|
NP_597681.4:p.Gly16318Ala
|
|
NR_038271.1:n.447-740C>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-12012C>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.74669G>C
(TTN)
|
XP_011510031.1:p.Gly24890Ala
|
|
XM_011511730.1:c.48563G>C
(TTN)
|
XP_011510032.1:p.Gly16188Ala
|
|
XM_011511731.1:c.48422G>C
(TTN)
|
XP_011510033.1:p.Gly16141Ala
|
|
XM_017004819.1:c.74465G>C
(TTN)
|
XP_016860308.1:p.Gly24822Ala
|
|
XM_017004820.1:c.69863G>C
(TTN)
|
XP_016860309.1:p.Gly23288Ala
|
|
XM_017004821.1:c.69860G>C
(TTN)
|
XP_016860310.1:p.Gly23287Ala
|
|
XM_017004822.1:c.66902G>C
(TTN)
|
XP_016860311.1:p.Gly22301Ala
|
|
XM_017004823.1:c.48518G>C
(TTN)
|
XP_016860312.1:p.Gly16173Ala
|
|
XM_024453094.1:c.70013G>C
(TTN)
|
XP_024308862.1:p.Gly23338Ala
|
|
XM_024453095.1:c.70010G>C
(TTN)
|
XP_024308863.1:p.Gly23337Ala
|
|
XM_024453096.1:c.69443G>C
(TTN)
|
XP_024308864.1:p.Gly23148Ala
|
|
XM_024453097.1:c.66785G>C
(TTN)
|
XP_024308865.1:p.Gly22262Ala
|
|
XM_024453098.1:c.66704G>C
(TTN)
|
XP_024308866.1:p.Gly22235Ala
|
|
XM_024453099.1:c.48467G>C
(TTN)
|
XP_024308867.1:p.Gly16156Ala
|
|
XM_024453100.1:c.38321G>C
(TTN)
|
XP_024308868.1:p.Gly12774Ala
|
|