ENST00000342992.11:c.96683A>G
(TTN)
|
ENSP00000343764.6:p.Glu32228Gly
|
|
ENST00000342175.11:c.77768A>G
(TTN)
|
ENSP00000340554.6:p.Glu25923Gly
|
|
ENST00000359218.10:c.77567A>G
(TTN)
|
ENSP00000352154.5:p.Glu25856Gly
|
|
ENST00000342175.10:c.77768A>G
(TTN)
|
ENSP00000340554.6:p.Glu25923Gly
|
|
ENST00000342992.10:c.96683A>G
(TTN)
|
ENSP00000343764.6:p.Glu32228Gly
|
|
ENST00000359218.9:c.77567A>G
(TTN)
|
ENSP00000352154.5:p.Glu25856Gly
|
|
ENST00000460472.6:c.77192A>G
(TTN)
|
ENSP00000434586.1:p.Glu25731Gly
|
|
ENST00000589042.5:c.104387A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu34796Gly
|
|
ENST00000591111.5:c.99464A>G
(TTN)
|
ENSP00000465570.1:p.Glu33155Gly
|
|
ENST00000615779.4:c.99464A>G
(TTN)
|
ENSP00000483597.1:p.Glu33155Gly
|
|
NM_001256850.1:c.99464A>G
(TTN)
|
NP_001243779.1:p.Glu33155Gly
|
|
NM_001267550.2:c.104387A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Glu34796Gly
|
|
NM_003319.4:c.77192A>G
(TTN)
|
NP_003310.4:p.Glu25731Gly
|
|
NM_133378.4:c.96683A>G
(TTN)
|
NP_596869.4:p.Glu32228Gly
|
|
NM_133432.3:c.77567A>G
(TTN)
|
NP_597676.3:p.Glu25856Gly
|
|
NM_133437.4:c.77768A>G
(TTN)
|
NP_597681.4:p.Glu25923Gly
|
|
NR_038271.1:n.446+8592T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3504T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.103484A>G
(TTN)
|
XP_011510031.1:p.Glu34495Gly
|
|
XM_011511730.1:c.77378A>G
(TTN)
|
XP_011510032.1:p.Glu25793Gly
|
|
XM_011511731.1:c.77237A>G
(TTN)
|
XP_011510033.1:p.Glu25746Gly
|
|
XM_017004819.1:c.103280A>G
(TTN)
|
XP_016860308.1:p.Glu34427Gly
|
|
XM_017004820.1:c.98678A>G
(TTN)
|
XP_016860309.1:p.Glu32893Gly
|
|
XM_017004821.1:c.98675A>G
(TTN)
|
XP_016860310.1:p.Glu32892Gly
|
|
XM_017004822.1:c.95717A>G
(TTN)
|
XP_016860311.1:p.Glu31906Gly
|
|
XM_017004823.1:c.77333A>G
(TTN)
|
XP_016860312.1:p.Glu25778Gly
|
|
XM_024453094.1:c.98828A>G
(TTN)
|
XP_024308862.1:p.Glu32943Gly
|
|
XM_024453095.1:c.98825A>G
(TTN)
|
XP_024308863.1:p.Glu32942Gly
|
|
XM_024453096.1:c.98258A>G
(TTN)
|
XP_024308864.1:p.Glu32753Gly
|
|
XM_024453097.1:c.95600A>G
(TTN)
|
XP_024308865.1:p.Glu31867Gly
|
|
XM_024453098.1:c.95519A>G
(TTN)
|
XP_024308866.1:p.Glu31840Gly
|
|
XM_024453099.1:c.77282A>G
(TTN)
|
XP_024308867.1:p.Glu25761Gly
|
|
XM_024453100.1:c.67136A>G
(TTN)
|
XP_024308868.1:p.Glu22379Gly
|
|