ENST00000342992.11:c.86180G>C
(TTN)
|
ENSP00000343764.6:p.Gly28727Ala
|
|
ENST00000342175.11:c.67265G>C
(TTN)
|
ENSP00000340554.6:p.Gly22422Ala
|
|
ENST00000359218.10:c.67064G>C
(TTN)
|
ENSP00000352154.5:p.Gly22355Ala
|
|
ENST00000342175.10:c.67265G>C
(TTN)
|
ENSP00000340554.6:p.Gly22422Ala
|
|
ENST00000342992.10:c.86180G>C
(TTN)
|
ENSP00000343764.6:p.Gly28727Ala
|
|
ENST00000359218.9:c.67064G>C
(TTN)
|
ENSP00000352154.5:p.Gly22355Ala
|
|
ENST00000460472.6:c.66689G>C
(TTN)
|
ENSP00000434586.1:p.Gly22230Ala
|
|
ENST00000589042.5:c.93884G>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gly31295Ala
|
|
ENST00000591111.5:c.88961G>C
(TTN)
|
ENSP00000465570.1:p.Gly29654Ala
|
|
ENST00000615779.4:c.88961G>C
(TTN)
|
ENSP00000483597.1:p.Gly29654Ala
|
|
NM_001256850.1:c.88961G>C
(TTN)
|
NP_001243779.1:p.Gly29654Ala
|
|
NM_001267550.2:c.93884G>C
(TTN)
MANE Select
|
NP_001254479.2:p.Gly31295Ala
|
|
NM_003319.4:c.66689G>C
(TTN)
|
NP_003310.4:p.Gly22230Ala
|
|
NM_133378.4:c.86180G>C
(TTN)
|
NP_596869.4:p.Gly28727Ala
|
|
NM_133432.3:c.67064G>C
(TTN)
|
NP_597676.3:p.Gly22355Ala
|
|
NM_133437.4:c.67265G>C
(TTN)
|
NP_597681.4:p.Gly22422Ala
|
|
NR_038271.1:n.447-23558C>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+5381C>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.92981G>C
(TTN)
|
XP_011510031.1:p.Gly30994Ala
|
|
XM_011511730.1:c.66875G>C
(TTN)
|
XP_011510032.1:p.Gly22292Ala
|
|
XM_011511731.1:c.66734G>C
(TTN)
|
XP_011510033.1:p.Gly22245Ala
|
|
XM_017004819.1:c.92777G>C
(TTN)
|
XP_016860308.1:p.Gly30926Ala
|
|
XM_017004820.1:c.88175G>C
(TTN)
|
XP_016860309.1:p.Gly29392Ala
|
|
XM_017004821.1:c.88172G>C
(TTN)
|
XP_016860310.1:p.Gly29391Ala
|
|
XM_017004822.1:c.85214G>C
(TTN)
|
XP_016860311.1:p.Gly28405Ala
|
|
XM_017004823.1:c.66830G>C
(TTN)
|
XP_016860312.1:p.Gly22277Ala
|
|
XM_024453094.1:c.88325G>C
(TTN)
|
XP_024308862.1:p.Gly29442Ala
|
|
XM_024453095.1:c.88322G>C
(TTN)
|
XP_024308863.1:p.Gly29441Ala
|
|
XM_024453096.1:c.87755G>C
(TTN)
|
XP_024308864.1:p.Gly29252Ala
|
|
XM_024453097.1:c.85097G>C
(TTN)
|
XP_024308865.1:p.Gly28366Ala
|
|
XM_024453098.1:c.85016G>C
(TTN)
|
XP_024308866.1:p.Gly28339Ala
|
|
XM_024453099.1:c.66779G>C
(TTN)
|
XP_024308867.1:p.Gly22260Ala
|
|
XM_024453100.1:c.56633G>C
(TTN)
|
XP_024308868.1:p.Gly18878Ala
|
|