ENST00000342992.11:c.88136A>G
(TTN)
|
ENSP00000343764.6:p.Glu29379Gly
|
|
ENST00000342175.11:c.69221A>G
(TTN)
|
ENSP00000340554.6:p.Glu23074Gly
|
|
ENST00000359218.10:c.69020A>G
(TTN)
|
ENSP00000352154.5:p.Glu23007Gly
|
|
ENST00000342175.10:c.69221A>G
(TTN)
|
ENSP00000340554.6:p.Glu23074Gly
|
|
ENST00000342992.10:c.88136A>G
(TTN)
|
ENSP00000343764.6:p.Glu29379Gly
|
|
ENST00000359218.9:c.69020A>G
(TTN)
|
ENSP00000352154.5:p.Glu23007Gly
|
|
ENST00000460472.6:c.68645A>G
(TTN)
|
ENSP00000434586.1:p.Glu22882Gly
|
|
ENST00000589042.5:c.95840A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu31947Gly
|
|
ENST00000591111.5:c.90917A>G
(TTN)
|
ENSP00000465570.1:p.Glu30306Gly
|
|
ENST00000615779.4:c.90917A>G
(TTN)
|
ENSP00000483597.1:p.Glu30306Gly
|
|
NM_001256850.1:c.90917A>G
(TTN)
|
NP_001243779.1:p.Glu30306Gly
|
|
NM_001267550.2:c.95840A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Glu31947Gly
|
|
NM_003319.4:c.68645A>G
(TTN)
|
NP_003310.4:p.Glu22882Gly
|
|
NM_133378.4:c.88136A>G
(TTN)
|
NP_596869.4:p.Glu29379Gly
|
|
NM_133432.3:c.69020A>G
(TTN)
|
NP_597676.3:p.Glu23007Gly
|
|
NM_133437.4:c.69221A>G
(TTN)
|
NP_597681.4:p.Glu23074Gly
|
|
NR_038271.1:n.446+20753T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+2028T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.94937A>G
(TTN)
|
XP_011510031.1:p.Glu31646Gly
|
|
XM_011511730.1:c.68831A>G
(TTN)
|
XP_011510032.1:p.Glu22944Gly
|
|
XM_011511731.1:c.68690A>G
(TTN)
|
XP_011510033.1:p.Glu22897Gly
|
|
XM_017004819.1:c.94733A>G
(TTN)
|
XP_016860308.1:p.Glu31578Gly
|
|
XM_017004820.1:c.90131A>G
(TTN)
|
XP_016860309.1:p.Glu30044Gly
|
|
XM_017004821.1:c.90128A>G
(TTN)
|
XP_016860310.1:p.Glu30043Gly
|
|
XM_017004822.1:c.87170A>G
(TTN)
|
XP_016860311.1:p.Glu29057Gly
|
|
XM_017004823.1:c.68786A>G
(TTN)
|
XP_016860312.1:p.Glu22929Gly
|
|
XM_024453094.1:c.90281A>G
(TTN)
|
XP_024308862.1:p.Glu30094Gly
|
|
XM_024453095.1:c.90278A>G
(TTN)
|
XP_024308863.1:p.Glu30093Gly
|
|
XM_024453096.1:c.89711A>G
(TTN)
|
XP_024308864.1:p.Glu29904Gly
|
|
XM_024453097.1:c.87053A>G
(TTN)
|
XP_024308865.1:p.Glu29018Gly
|
|
XM_024453098.1:c.86972A>G
(TTN)
|
XP_024308866.1:p.Glu28991Gly
|
|
XM_024453099.1:c.68735A>G
(TTN)
|
XP_024308867.1:p.Glu22912Gly
|
|
XM_024453100.1:c.58589A>G
(TTN)
|
XP_024308868.1:p.Glu19530Gly
|
|