ENST00000342992.11:c.96727G>A
(TTN)
|
ENSP00000343764.6:p.Glu32243Lys
|
|
ENST00000342175.11:c.77812G>A
(TTN)
|
ENSP00000340554.6:p.Glu25938Lys
|
|
ENST00000359218.10:c.77611G>A
(TTN)
|
ENSP00000352154.5:p.Glu25871Lys
|
|
ENST00000342175.10:c.77812G>A
(TTN)
|
ENSP00000340554.6:p.Glu25938Lys
|
|
ENST00000342992.10:c.96727G>A
(TTN)
|
ENSP00000343764.6:p.Glu32243Lys
|
|
ENST00000359218.9:c.77611G>A
(TTN)
|
ENSP00000352154.5:p.Glu25871Lys
|
|
ENST00000460472.6:c.77236G>A
(TTN)
|
ENSP00000434586.1:p.Glu25746Lys
|
|
ENST00000589042.5:c.104431G>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu34811Lys
|
|
ENST00000591111.5:c.99508G>A
(TTN)
|
ENSP00000465570.1:p.Glu33170Lys
|
|
ENST00000615779.4:c.99508G>A
(TTN)
|
ENSP00000483597.1:p.Glu33170Lys
|
|
NM_001256850.1:c.99508G>A
(TTN)
|
NP_001243779.1:p.Glu33170Lys
|
|
NM_001267550.2:c.104431G>A
(TTN)
MANE Select
|
NP_001254479.2:p.Glu34811Lys
|
|
NM_003319.4:c.77236G>A
(TTN)
|
NP_003310.4:p.Glu25746Lys
|
|
NM_133378.4:c.96727G>A
(TTN)
|
NP_596869.4:p.Glu32243Lys
|
|
NM_133432.3:c.77611G>A
(TTN)
|
NP_597676.3:p.Glu25871Lys
|
|
NM_133437.4:c.77812G>A
(TTN)
|
NP_597681.4:p.Glu25938Lys
|
|
NR_038271.1:n.446+8548C>T
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3548C>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.103528G>A
(TTN)
|
XP_011510031.1:p.Glu34510Lys
|
|
XM_011511730.1:c.77422G>A
(TTN)
|
XP_011510032.1:p.Glu25808Lys
|
|
XM_011511731.1:c.77281G>A
(TTN)
|
XP_011510033.1:p.Glu25761Lys
|
|
XM_017004819.1:c.103324G>A
(TTN)
|
XP_016860308.1:p.Glu34442Lys
|
|
XM_017004820.1:c.98722G>A
(TTN)
|
XP_016860309.1:p.Glu32908Lys
|
|
XM_017004821.1:c.98719G>A
(TTN)
|
XP_016860310.1:p.Glu32907Lys
|
|
XM_017004822.1:c.95761G>A
(TTN)
|
XP_016860311.1:p.Glu31921Lys
|
|
XM_017004823.1:c.77377G>A
(TTN)
|
XP_016860312.1:p.Glu25793Lys
|
|
XM_024453094.1:c.98872G>A
(TTN)
|
XP_024308862.1:p.Glu32958Lys
|
|
XM_024453095.1:c.98869G>A
(TTN)
|
XP_024308863.1:p.Glu32957Lys
|
|
XM_024453096.1:c.98302G>A
(TTN)
|
XP_024308864.1:p.Glu32768Lys
|
|
XM_024453097.1:c.95644G>A
(TTN)
|
XP_024308865.1:p.Glu31882Lys
|
|
XM_024453098.1:c.95563G>A
(TTN)
|
XP_024308866.1:p.Glu31855Lys
|
|
XM_024453099.1:c.77326G>A
(TTN)
|
XP_024308867.1:p.Glu25776Lys
|
|
XM_024453100.1:c.67180G>A
(TTN)
|
XP_024308868.1:p.Glu22394Lys
|
|