ENST00000342992.11:c.98485C>G
(TTN)
|
ENSP00000343764.6:p.Gln32829Glu
|
|
ENST00000342175.11:c.79570C>G
(TTN)
|
ENSP00000340554.6:p.Gln26524Glu
|
|
ENST00000359218.10:c.79369C>G
(TTN)
|
ENSP00000352154.5:p.Gln26457Glu
|
|
ENST00000342175.10:c.79570C>G
(TTN)
|
ENSP00000340554.6:p.Gln26524Glu
|
|
ENST00000342992.10:c.98485C>G
(TTN)
|
ENSP00000343764.6:p.Gln32829Glu
|
|
ENST00000359218.9:c.79369C>G
(TTN)
|
ENSP00000352154.5:p.Gln26457Glu
|
|
ENST00000460472.6:c.78994C>G
(TTN)
|
ENSP00000434586.1:p.Gln26332Glu
|
|
ENST00000589042.5:c.106189C>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gln35397Glu
|
|
ENST00000591111.5:c.101266C>G
(TTN)
|
ENSP00000465570.1:p.Gln33756Glu
|
|
ENST00000615779.4:c.101266C>G
(TTN)
|
ENSP00000483597.1:p.Gln33756Glu
|
|
NM_001256850.1:c.101266C>G
(TTN)
|
NP_001243779.1:p.Gln33756Glu
|
|
NM_001267550.2:c.106189C>G
(TTN)
MANE Select
|
NP_001254479.2:p.Gln35397Glu
|
|
NM_003319.4:c.78994C>G
(TTN)
|
NP_003310.4:p.Gln26332Glu
|
|
NM_133378.4:c.98485C>G
(TTN)
|
NP_596869.4:p.Gln32829Glu
|
|
NM_133432.3:c.79369C>G
(TTN)
|
NP_597676.3:p.Gln26457Glu
|
|
NM_133437.4:c.79570C>G
(TTN)
|
NP_597681.4:p.Gln26524Glu
|
|
NR_038271.1:n.446+6790G>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5306G>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.105286C>G
(TTN)
|
XP_011510031.1:p.Gln35096Glu
|
|
XM_011511730.1:c.79180C>G
(TTN)
|
XP_011510032.1:p.Gln26394Glu
|
|
XM_011511731.1:c.79039C>G
(TTN)
|
XP_011510033.1:p.Gln26347Glu
|
|
XM_017004819.1:c.105082C>G
(TTN)
|
XP_016860308.1:p.Gln35028Glu
|
|
XM_017004820.1:c.100480C>G
(TTN)
|
XP_016860309.1:p.Gln33494Glu
|
|
XM_017004821.1:c.100477C>G
(TTN)
|
XP_016860310.1:p.Gln33493Glu
|
|
XM_017004822.1:c.97519C>G
(TTN)
|
XP_016860311.1:p.Gln32507Glu
|
|
XM_017004823.1:c.79135C>G
(TTN)
|
XP_016860312.1:p.Gln26379Glu
|
|
XM_024453094.1:c.100630C>G
(TTN)
|
XP_024308862.1:p.Gln33544Glu
|
|
XM_024453095.1:c.100627C>G
(TTN)
|
XP_024308863.1:p.Gln33543Glu
|
|
XM_024453096.1:c.100060C>G
(TTN)
|
XP_024308864.1:p.Gln33354Glu
|
|
XM_024453097.1:c.97402C>G
(TTN)
|
XP_024308865.1:p.Gln32468Glu
|
|
XM_024453098.1:c.97321C>G
(TTN)
|
XP_024308866.1:p.Gln32441Glu
|
|
XM_024453099.1:c.79084C>G
(TTN)
|
XP_024308867.1:p.Gln26362Glu
|
|
XM_024453100.1:c.68938C>G
(TTN)
|
XP_024308868.1:p.Gln22980Glu
|
|