ENST00000342992.11:c.88325A>C
(TTN)
|
ENSP00000343764.6:p.Glu29442Ala
|
|
ENST00000342175.11:c.69410A>C
(TTN)
|
ENSP00000340554.6:p.Glu23137Ala
|
|
ENST00000359218.10:c.69209A>C
(TTN)
|
ENSP00000352154.5:p.Glu23070Ala
|
|
ENST00000342175.10:c.69410A>C
(TTN)
|
ENSP00000340554.6:p.Glu23137Ala
|
|
ENST00000342992.10:c.88325A>C
(TTN)
|
ENSP00000343764.6:p.Glu29442Ala
|
|
ENST00000359218.9:c.69209A>C
(TTN)
|
ENSP00000352154.5:p.Glu23070Ala
|
|
ENST00000460472.6:c.68834A>C
(TTN)
|
ENSP00000434586.1:p.Glu22945Ala
|
|
ENST00000589042.5:c.96029A>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu32010Ala
|
|
ENST00000591111.5:c.91106A>C
(TTN)
|
ENSP00000465570.1:p.Glu30369Ala
|
|
ENST00000615779.4:c.91106A>C
(TTN)
|
ENSP00000483597.1:p.Glu30369Ala
|
|
NM_001256850.1:c.91106A>C
(TTN)
|
NP_001243779.1:p.Glu30369Ala
|
|
NM_001267550.2:c.96029A>C
(TTN)
MANE Select
|
NP_001254479.2:p.Glu32010Ala
|
|
NM_003319.4:c.68834A>C
(TTN)
|
NP_003310.4:p.Glu22945Ala
|
|
NM_133378.4:c.88325A>C
(TTN)
|
NP_596869.4:p.Glu29442Ala
|
|
NM_133432.3:c.69209A>C
(TTN)
|
NP_597676.3:p.Glu23070Ala
|
|
NM_133437.4:c.69410A>C
(TTN)
|
NP_597681.4:p.Glu23137Ala
|
|
NR_038271.1:n.446+20479T>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+1754T>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.95126A>C
(TTN)
|
XP_011510031.1:p.Glu31709Ala
|
|
XM_011511730.1:c.69020A>C
(TTN)
|
XP_011510032.1:p.Glu23007Ala
|
|
XM_011511731.1:c.68879A>C
(TTN)
|
XP_011510033.1:p.Glu22960Ala
|
|
XM_017004819.1:c.94922A>C
(TTN)
|
XP_016860308.1:p.Glu31641Ala
|
|
XM_017004820.1:c.90320A>C
(TTN)
|
XP_016860309.1:p.Glu30107Ala
|
|
XM_017004821.1:c.90317A>C
(TTN)
|
XP_016860310.1:p.Glu30106Ala
|
|
XM_017004822.1:c.87359A>C
(TTN)
|
XP_016860311.1:p.Glu29120Ala
|
|
XM_017004823.1:c.68975A>C
(TTN)
|
XP_016860312.1:p.Glu22992Ala
|
|
XM_024453094.1:c.90470A>C
(TTN)
|
XP_024308862.1:p.Glu30157Ala
|
|
XM_024453095.1:c.90467A>C
(TTN)
|
XP_024308863.1:p.Glu30156Ala
|
|
XM_024453096.1:c.89900A>C
(TTN)
|
XP_024308864.1:p.Glu29967Ala
|
|
XM_024453097.1:c.87242A>C
(TTN)
|
XP_024308865.1:p.Glu29081Ala
|
|
XM_024453098.1:c.87161A>C
(TTN)
|
XP_024308866.1:p.Glu29054Ala
|
|
XM_024453099.1:c.68924A>C
(TTN)
|
XP_024308867.1:p.Glu22975Ala
|
|
XM_024453100.1:c.58778A>C
(TTN)
|
XP_024308868.1:p.Glu19593Ala
|
|