ENST00000342992.11:c.96663A>T
(TTN)
|
ENSP00000343764.6:p.Glu32221Asp
|
|
ENST00000342175.11:c.77748A>T
(TTN)
|
ENSP00000340554.6:p.Glu25916Asp
|
|
ENST00000359218.10:c.77547A>T
(TTN)
|
ENSP00000352154.5:p.Glu25849Asp
|
|
ENST00000342175.10:c.77748A>T
(TTN)
|
ENSP00000340554.6:p.Glu25916Asp
|
|
ENST00000342992.10:c.96663A>T
(TTN)
|
ENSP00000343764.6:p.Glu32221Asp
|
|
ENST00000359218.9:c.77547A>T
(TTN)
|
ENSP00000352154.5:p.Glu25849Asp
|
|
ENST00000460472.6:c.77172A>T
(TTN)
|
ENSP00000434586.1:p.Glu25724Asp
|
|
ENST00000589042.5:c.104367A>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu34789Asp
|
|
ENST00000591111.5:c.99444A>T
(TTN)
|
ENSP00000465570.1:p.Glu33148Asp
|
|
ENST00000615779.4:c.99444A>T
(TTN)
|
ENSP00000483597.1:p.Glu33148Asp
|
|
NM_001256850.1:c.99444A>T
(TTN)
|
NP_001243779.1:p.Glu33148Asp
|
|
NM_001267550.2:c.104367A>T
(TTN)
MANE Select
|
NP_001254479.2:p.Glu34789Asp
|
|
NM_003319.4:c.77172A>T
(TTN)
|
NP_003310.4:p.Glu25724Asp
|
|
NM_133378.4:c.96663A>T
(TTN)
|
NP_596869.4:p.Glu32221Asp
|
|
NM_133432.3:c.77547A>T
(TTN)
|
NP_597676.3:p.Glu25849Asp
|
|
NM_133437.4:c.77748A>T
(TTN)
|
NP_597681.4:p.Glu25916Asp
|
|
NR_038271.1:n.446+8612T>A
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3484T>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.103464A>T
(TTN)
|
XP_011510031.1:p.Glu34488Asp
|
|
XM_011511730.1:c.77358A>T
(TTN)
|
XP_011510032.1:p.Glu25786Asp
|
|
XM_011511731.1:c.77217A>T
(TTN)
|
XP_011510033.1:p.Glu25739Asp
|
|
XM_017004819.1:c.103260A>T
(TTN)
|
XP_016860308.1:p.Glu34420Asp
|
|
XM_017004820.1:c.98658A>T
(TTN)
|
XP_016860309.1:p.Glu32886Asp
|
|
XM_017004821.1:c.98655A>T
(TTN)
|
XP_016860310.1:p.Glu32885Asp
|
|
XM_017004822.1:c.95697A>T
(TTN)
|
XP_016860311.1:p.Glu31899Asp
|
|
XM_017004823.1:c.77313A>T
(TTN)
|
XP_016860312.1:p.Glu25771Asp
|
|
XM_024453094.1:c.98808A>T
(TTN)
|
XP_024308862.1:p.Glu32936Asp
|
|
XM_024453095.1:c.98805A>T
(TTN)
|
XP_024308863.1:p.Glu32935Asp
|
|
XM_024453096.1:c.98238A>T
(TTN)
|
XP_024308864.1:p.Glu32746Asp
|
|
XM_024453097.1:c.95580A>T
(TTN)
|
XP_024308865.1:p.Glu31860Asp
|
|
XM_024453098.1:c.95499A>T
(TTN)
|
XP_024308866.1:p.Glu31833Asp
|
|
XM_024453099.1:c.77262A>T
(TTN)
|
XP_024308867.1:p.Glu25754Asp
|
|
XM_024453100.1:c.67116A>T
(TTN)
|
XP_024308868.1:p.Glu22372Asp
|
|