ENST00000342992.11:c.82640T>G
(TTN)
|
ENSP00000343764.6:p.Val27547Gly
|
|
ENST00000342175.11:c.63725T>G
(TTN)
|
ENSP00000340554.6:p.Val21242Gly
|
|
ENST00000359218.10:c.63524T>G
(TTN)
|
ENSP00000352154.5:p.Val21175Gly
|
|
ENST00000342175.10:c.63725T>G
(TTN)
|
ENSP00000340554.6:p.Val21242Gly
|
|
ENST00000342992.10:c.82640T>G
(TTN)
|
ENSP00000343764.6:p.Val27547Gly
|
|
ENST00000359218.9:c.63524T>G
(TTN)
|
ENSP00000352154.5:p.Val21175Gly
|
|
ENST00000460472.6:c.63149T>G
(TTN)
|
ENSP00000434586.1:p.Val21050Gly
|
|
ENST00000589042.5:c.90344T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Val30115Gly
|
|
ENST00000591111.5:c.85421T>G
(TTN)
|
ENSP00000465570.1:p.Val28474Gly
|
|
ENST00000615779.4:c.85421T>G
(TTN)
|
ENSP00000483597.1:p.Val28474Gly
|
|
NM_001256850.1:c.85421T>G
(TTN)
|
NP_001243779.1:p.Val28474Gly
|
|
NM_001267550.2:c.90344T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Val30115Gly
|
|
NM_003319.4:c.63149T>G
(TTN)
|
NP_003310.4:p.Val21050Gly
|
|
NM_133378.4:c.82640T>G
(TTN)
|
NP_596869.4:p.Val27547Gly
|
|
NM_133432.3:c.63524T>G
(TTN)
|
NP_597676.3:p.Val21175Gly
|
|
NM_133437.4:c.63725T>G
(TTN)
|
NP_597681.4:p.Val21242Gly
|
|
NR_038271.1:n.447-18744A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+10195A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.89441T>G
(TTN)
|
XP_011510031.1:p.Val29814Gly
|
|
XM_011511730.1:c.63335T>G
(TTN)
|
XP_011510032.1:p.Val21112Gly
|
|
XM_011511731.1:c.63194T>G
(TTN)
|
XP_011510033.1:p.Val21065Gly
|
|
XM_017004819.1:c.89237T>G
(TTN)
|
XP_016860308.1:p.Val29746Gly
|
|
XM_017004820.1:c.84635T>G
(TTN)
|
XP_016860309.1:p.Val28212Gly
|
|
XM_017004821.1:c.84632T>G
(TTN)
|
XP_016860310.1:p.Val28211Gly
|
|
XM_017004822.1:c.81674T>G
(TTN)
|
XP_016860311.1:p.Val27225Gly
|
|
XM_017004823.1:c.63290T>G
(TTN)
|
XP_016860312.1:p.Val21097Gly
|
|
XM_024453094.1:c.84785T>G
(TTN)
|
XP_024308862.1:p.Val28262Gly
|
|
XM_024453095.1:c.84782T>G
(TTN)
|
XP_024308863.1:p.Val28261Gly
|
|
XM_024453096.1:c.84215T>G
(TTN)
|
XP_024308864.1:p.Val28072Gly
|
|
XM_024453097.1:c.81557T>G
(TTN)
|
XP_024308865.1:p.Val27186Gly
|
|
XM_024453098.1:c.81476T>G
(TTN)
|
XP_024308866.1:p.Val27159Gly
|
|
XM_024453099.1:c.63239T>G
(TTN)
|
XP_024308867.1:p.Val21080Gly
|
|
XM_024453100.1:c.53093T>G
(TTN)
|
XP_024308868.1:p.Val17698Gly
|
|