ENST00000342992.11:c.98391T>C
(TTN)
|
ENSP00000343764.6:p.Gly32797=
|
|
ENST00000342175.11:c.79476T>C
(TTN)
|
ENSP00000340554.6:p.Gly26492=
|
|
ENST00000359218.10:c.79275T>C
(TTN)
|
ENSP00000352154.5:p.Gly26425=
|
|
ENST00000342175.10:c.79476T>C
(TTN)
|
ENSP00000340554.6:p.Gly26492=
|
|
ENST00000342992.10:c.98391T>C
(TTN)
|
ENSP00000343764.6:p.Gly32797=
|
|
ENST00000359218.9:c.79275T>C
(TTN)
|
ENSP00000352154.5:p.Gly26425=
|
|
ENST00000460472.6:c.78900T>C
(TTN)
|
ENSP00000434586.1:p.Gly26300=
|
|
ENST00000589042.5:c.106095T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gly35365=
|
|
ENST00000591111.5:c.101172T>C
(TTN)
|
ENSP00000465570.1:p.Gly33724=
|
|
ENST00000615779.4:c.101172T>C
(TTN)
|
ENSP00000483597.1:p.Gly33724=
|
|
NM_001256850.1:c.101172T>C
(TTN)
|
NP_001243779.1:p.Gly33724=
|
|
NM_001267550.2:c.106095T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Gly35365=
|
|
NM_003319.4:c.78900T>C
(TTN)
|
NP_003310.4:p.Gly26300=
|
|
NM_133378.4:c.98391T>C
(TTN)
|
NP_596869.4:p.Gly32797=
|
|
NM_133432.3:c.79275T>C
(TTN)
|
NP_597676.3:p.Gly26425=
|
|
NM_133437.4:c.79476T>C
(TTN)
|
NP_597681.4:p.Gly26492=
|
|
NR_038271.1:n.446+6884A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5212A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.105192T>C
(TTN)
|
XP_011510031.1:p.Gly35064=
|
|
XM_011511730.1:c.79086T>C
(TTN)
|
XP_011510032.1:p.Gly26362=
|
|
XM_011511731.1:c.78945T>C
(TTN)
|
XP_011510033.1:p.Gly26315=
|
|
XM_017004819.1:c.104988T>C
(TTN)
|
XP_016860308.1:p.Gly34996=
|
|
XM_017004820.1:c.100386T>C
(TTN)
|
XP_016860309.1:p.Gly33462=
|
|
XM_017004821.1:c.100383T>C
(TTN)
|
XP_016860310.1:p.Gly33461=
|
|
XM_017004822.1:c.97425T>C
(TTN)
|
XP_016860311.1:p.Gly32475=
|
|
XM_017004823.1:c.79041T>C
(TTN)
|
XP_016860312.1:p.Gly26347=
|
|
XM_024453094.1:c.100536T>C
(TTN)
|
XP_024308862.1:p.Gly33512=
|
|
XM_024453095.1:c.100533T>C
(TTN)
|
XP_024308863.1:p.Gly33511=
|
|
XM_024453096.1:c.99966T>C
(TTN)
|
XP_024308864.1:p.Gly33322=
|
|
XM_024453097.1:c.97308T>C
(TTN)
|
XP_024308865.1:p.Gly32436=
|
|
XM_024453098.1:c.97227T>C
(TTN)
|
XP_024308866.1:p.Gly32409=
|
|
XM_024453099.1:c.78990T>C
(TTN)
|
XP_024308867.1:p.Gly26330=
|
|
XM_024453100.1:c.68844T>C
(TTN)
|
XP_024308868.1:p.Gly22948=
|
|