ENST00000342992.11:c.96873G>A
(TTN)
|
ENSP00000343764.6:p.Arg32291=
|
|
ENST00000342175.11:c.77958G>A
(TTN)
|
ENSP00000340554.6:p.Arg25986=
|
|
ENST00000359218.10:c.77757G>A
(TTN)
|
ENSP00000352154.5:p.Arg25919=
|
|
ENST00000342175.10:c.77958G>A
(TTN)
|
ENSP00000340554.6:p.Arg25986=
|
|
ENST00000342992.10:c.96873G>A
(TTN)
|
ENSP00000343764.6:p.Arg32291=
|
|
ENST00000359218.9:c.77757G>A
(TTN)
|
ENSP00000352154.5:p.Arg25919=
|
|
ENST00000460472.6:c.77382G>A
(TTN)
|
ENSP00000434586.1:p.Arg25794=
|
|
ENST00000589042.5:c.104577G>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Arg34859=
|
|
ENST00000591111.5:c.99654G>A
(TTN)
|
ENSP00000465570.1:p.Arg33218=
|
|
ENST00000615779.4:c.99654G>A
(TTN)
|
ENSP00000483597.1:p.Arg33218=
|
|
NM_001256850.1:c.99654G>A
(TTN)
|
NP_001243779.1:p.Arg33218=
|
|
NM_001267550.2:c.104577G>A
(TTN)
MANE Select
|
NP_001254479.2:p.Arg34859=
|
|
NM_003319.4:c.77382G>A
(TTN)
|
NP_003310.4:p.Arg25794=
|
|
NM_133378.4:c.96873G>A
(TTN)
|
NP_596869.4:p.Arg32291=
|
|
NM_133432.3:c.77757G>A
(TTN)
|
NP_597676.3:p.Arg25919=
|
|
NM_133437.4:c.77958G>A
(TTN)
|
NP_597681.4:p.Arg25986=
|
|
NR_038271.1:n.446+8402C>T
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3694C>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.103674G>A
(TTN)
|
XP_011510031.1:p.Arg34558=
|
|
XM_011511730.1:c.77568G>A
(TTN)
|
XP_011510032.1:p.Arg25856=
|
|
XM_011511731.1:c.77427G>A
(TTN)
|
XP_011510033.1:p.Arg25809=
|
|
XM_017004819.1:c.103470G>A
(TTN)
|
XP_016860308.1:p.Arg34490=
|
|
XM_017004820.1:c.98868G>A
(TTN)
|
XP_016860309.1:p.Arg32956=
|
|
XM_017004821.1:c.98865G>A
(TTN)
|
XP_016860310.1:p.Arg32955=
|
|
XM_017004822.1:c.95907G>A
(TTN)
|
XP_016860311.1:p.Arg31969=
|
|
XM_017004823.1:c.77523G>A
(TTN)
|
XP_016860312.1:p.Arg25841=
|
|
XM_024453094.1:c.99018G>A
(TTN)
|
XP_024308862.1:p.Arg33006=
|
|
XM_024453095.1:c.99015G>A
(TTN)
|
XP_024308863.1:p.Arg33005=
|
|
XM_024453096.1:c.98448G>A
(TTN)
|
XP_024308864.1:p.Arg32816=
|
|
XM_024453097.1:c.95790G>A
(TTN)
|
XP_024308865.1:p.Arg31930=
|
|
XM_024453098.1:c.95709G>A
(TTN)
|
XP_024308866.1:p.Arg31903=
|
|
XM_024453099.1:c.77472G>A
(TTN)
|
XP_024308867.1:p.Arg25824=
|
|
XM_024453100.1:c.67326G>A
(TTN)
|
XP_024308868.1:p.Arg22442=
|
|