ENST00000342992.11:c.82516G>T
(TTN)
|
ENSP00000343764.6:p.Glu27506Ter
|
|
ENST00000342175.11:c.63601G>T
(TTN)
|
ENSP00000340554.6:p.Glu21201Ter
|
|
ENST00000359218.10:c.63400G>T
(TTN)
|
ENSP00000352154.5:p.Glu21134Ter
|
|
ENST00000342175.10:c.63601G>T
(TTN)
|
ENSP00000340554.6:p.Glu21201Ter
|
|
ENST00000342992.10:c.82516G>T
(TTN)
|
ENSP00000343764.6:p.Glu27506Ter
|
|
ENST00000359218.9:c.63400G>T
(TTN)
|
ENSP00000352154.5:p.Glu21134Ter
|
|
ENST00000460472.6:c.63025G>T
(TTN)
|
ENSP00000434586.1:p.Glu21009Ter
|
|
ENST00000589042.5:c.90220G>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu30074Ter
|
|
ENST00000591111.5:c.85297G>T
(TTN)
|
ENSP00000465570.1:p.Glu28433Ter
|
|
ENST00000615779.4:c.85297G>T
(TTN)
|
ENSP00000483597.1:p.Glu28433Ter
|
|
NM_001256850.1:c.85297G>T
(TTN)
|
NP_001243779.1:p.Glu28433Ter
|
|
NM_001267550.2:c.90220G>T
(TTN)
MANE Select
|
NP_001254479.2:p.Glu30074Ter
|
|
NM_003319.4:c.63025G>T
(TTN)
|
NP_003310.4:p.Glu21009Ter
|
|
NM_133378.4:c.82516G>T
(TTN)
|
NP_596869.4:p.Glu27506Ter
|
|
NM_133432.3:c.63400G>T
(TTN)
|
NP_597676.3:p.Glu21134Ter
|
|
NM_133437.4:c.63601G>T
(TTN)
|
NP_597681.4:p.Glu21201Ter
|
|
NR_038271.1:n.447-18620C>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+10319C>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.89317G>T
(TTN)
|
XP_011510031.1:p.Glu29773Ter
|
|
XM_011511730.1:c.63211G>T
(TTN)
|
XP_011510032.1:p.Glu21071Ter
|
|
XM_011511731.1:c.63070G>T
(TTN)
|
XP_011510033.1:p.Glu21024Ter
|
|
XM_017004819.1:c.89113G>T
(TTN)
|
XP_016860308.1:p.Glu29705Ter
|
|
XM_017004820.1:c.84511G>T
(TTN)
|
XP_016860309.1:p.Glu28171Ter
|
|
XM_017004821.1:c.84508G>T
(TTN)
|
XP_016860310.1:p.Glu28170Ter
|
|
XM_017004822.1:c.81550G>T
(TTN)
|
XP_016860311.1:p.Glu27184Ter
|
|
XM_017004823.1:c.63166G>T
(TTN)
|
XP_016860312.1:p.Glu21056Ter
|
|
XM_024453094.1:c.84661G>T
(TTN)
|
XP_024308862.1:p.Glu28221Ter
|
|
XM_024453095.1:c.84658G>T
(TTN)
|
XP_024308863.1:p.Glu28220Ter
|
|
XM_024453096.1:c.84091G>T
(TTN)
|
XP_024308864.1:p.Glu28031Ter
|
|
XM_024453097.1:c.81433G>T
(TTN)
|
XP_024308865.1:p.Glu27145Ter
|
|
XM_024453098.1:c.81352G>T
(TTN)
|
XP_024308866.1:p.Glu27118Ter
|
|
XM_024453099.1:c.63115G>T
(TTN)
|
XP_024308867.1:p.Glu21039Ter
|
|
XM_024453100.1:c.52969G>T
(TTN)
|
XP_024308868.1:p.Glu17657Ter
|
|