ENST00000342992.11:c.47362G>T
(TTN)
|
ENSP00000343764.6:p.Gly15788Cys
|
|
ENST00000342175.11:c.28447G>T
(TTN)
|
ENSP00000340554.6:p.Gly9483Cys
|
|
ENST00000359218.10:c.28246G>T
(TTN)
|
ENSP00000352154.5:p.Gly9416Cys
|
|
ENST00000342175.10:c.28447G>T
(TTN)
|
ENSP00000340554.6:p.Gly9483Cys
|
|
ENST00000342992.10:c.47362G>T
(TTN)
|
ENSP00000343764.6:p.Gly15788Cys
|
|
ENST00000359218.9:c.28246G>T
(TTN)
|
ENSP00000352154.5:p.Gly9416Cys
|
|
ENST00000460472.6:c.27871G>T
(TTN)
|
ENSP00000434586.1:p.Gly9291Cys
|
|
ENST00000589042.5:c.55066G>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gly18356Cys
|
|
ENST00000591111.5:c.50143G>T
(TTN)
|
ENSP00000465570.1:p.Gly16715Cys
|
|
ENST00000615779.4:c.50143G>T
(TTN)
|
ENSP00000483597.1:p.Gly16715Cys
|
|
NM_001256850.1:c.50143G>T
(TTN)
|
NP_001243779.1:p.Gly16715Cys
|
|
NM_001267550.2:c.55066G>T
(TTN)
MANE Select
|
NP_001254479.2:p.Gly18356Cys
|
|
NM_003319.4:c.27871G>T
(TTN)
|
NP_003310.4:p.Gly9291Cys
|
|
NM_133378.4:c.47362G>T
(TTN)
|
NP_596869.4:p.Gly15788Cys
|
|
NM_133432.3:c.28246G>T
(TTN)
|
NP_597676.3:p.Gly9416Cys
|
|
NM_133437.4:c.28447G>T
(TTN)
|
NP_597681.4:p.Gly9483Cys
|
|
NR_038271.1:n.682+4655C>A
(TTN-AS1)
|
|
|
NR_038272.1:n.3917+1669C>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.54163G>T
(TTN)
|
XP_011510031.1:p.Gly18055Cys
|
|
XM_011511730.1:c.28057G>T
(TTN)
|
XP_011510032.1:p.Gly9353Cys
|
|
XM_011511731.1:c.27916G>T
(TTN)
|
XP_011510033.1:p.Gly9306Cys
|
|
XM_017004819.1:c.53959G>T
(TTN)
|
XP_016860308.1:p.Gly17987Cys
|
|
XM_017004820.1:c.49357G>T
(TTN)
|
XP_016860309.1:p.Gly16453Cys
|
|
XM_017004821.1:c.49354G>T
(TTN)
|
XP_016860310.1:p.Gly16452Cys
|
|
XM_017004822.1:c.46396G>T
(TTN)
|
XP_016860311.1:p.Gly15466Cys
|
|
XM_017004823.1:c.28012G>T
(TTN)
|
XP_016860312.1:p.Gly9338Cys
|
|
XM_024453094.1:c.49507G>T
(TTN)
|
XP_024308862.1:p.Gly16503Cys
|
|
XM_024453095.1:c.49504G>T
(TTN)
|
XP_024308863.1:p.Gly16502Cys
|
|
XM_024453096.1:c.48937G>T
(TTN)
|
XP_024308864.1:p.Gly16313Cys
|
|
XM_024453097.1:c.46279G>T
(TTN)
|
XP_024308865.1:p.Gly15427Cys
|
|
XM_024453098.1:c.46198G>T
(TTN)
|
XP_024308866.1:p.Gly15400Cys
|
|
XM_024453099.1:c.27961G>T
(TTN)
|
XP_024308867.1:p.Gly9321Cys
|
|
XM_024453100.1:c.17815G>T
(TTN)
|
XP_024308868.1:p.Gly5939Cys
|
|