ENST00000342992.11:c.98448G>C
(TTN)
|
ENSP00000343764.6:p.Glu32816Asp
|
|
ENST00000342175.11:c.79533G>C
(TTN)
|
ENSP00000340554.6:p.Glu26511Asp
|
|
ENST00000359218.10:c.79332G>C
(TTN)
|
ENSP00000352154.5:p.Glu26444Asp
|
|
ENST00000342175.10:c.79533G>C
(TTN)
|
ENSP00000340554.6:p.Glu26511Asp
|
|
ENST00000342992.10:c.98448G>C
(TTN)
|
ENSP00000343764.6:p.Glu32816Asp
|
|
ENST00000359218.9:c.79332G>C
(TTN)
|
ENSP00000352154.5:p.Glu26444Asp
|
|
ENST00000460472.6:c.78957G>C
(TTN)
|
ENSP00000434586.1:p.Glu26319Asp
|
|
ENST00000589042.5:c.106152G>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu35384Asp
|
|
ENST00000591111.5:c.101229G>C
(TTN)
|
ENSP00000465570.1:p.Glu33743Asp
|
|
ENST00000615779.4:c.101229G>C
(TTN)
|
ENSP00000483597.1:p.Glu33743Asp
|
|
NM_001256850.1:c.101229G>C
(TTN)
|
NP_001243779.1:p.Glu33743Asp
|
|
NM_001267550.2:c.106152G>C
(TTN)
MANE Select
|
NP_001254479.2:p.Glu35384Asp
|
|
NM_003319.4:c.78957G>C
(TTN)
|
NP_003310.4:p.Glu26319Asp
|
|
NM_133378.4:c.98448G>C
(TTN)
|
NP_596869.4:p.Glu32816Asp
|
|
NM_133432.3:c.79332G>C
(TTN)
|
NP_597676.3:p.Glu26444Asp
|
|
NM_133437.4:c.79533G>C
(TTN)
|
NP_597681.4:p.Glu26511Asp
|
|
NR_038271.1:n.446+6827C>G
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5269C>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.105249G>C
(TTN)
|
XP_011510031.1:p.Glu35083Asp
|
|
XM_011511730.1:c.79143G>C
(TTN)
|
XP_011510032.1:p.Glu26381Asp
|
|
XM_011511731.1:c.79002G>C
(TTN)
|
XP_011510033.1:p.Glu26334Asp
|
|
XM_017004819.1:c.105045G>C
(TTN)
|
XP_016860308.1:p.Glu35015Asp
|
|
XM_017004820.1:c.100443G>C
(TTN)
|
XP_016860309.1:p.Glu33481Asp
|
|
XM_017004821.1:c.100440G>C
(TTN)
|
XP_016860310.1:p.Glu33480Asp
|
|
XM_017004822.1:c.97482G>C
(TTN)
|
XP_016860311.1:p.Glu32494Asp
|
|
XM_017004823.1:c.79098G>C
(TTN)
|
XP_016860312.1:p.Glu26366Asp
|
|
XM_024453094.1:c.100593G>C
(TTN)
|
XP_024308862.1:p.Glu33531Asp
|
|
XM_024453095.1:c.100590G>C
(TTN)
|
XP_024308863.1:p.Glu33530Asp
|
|
XM_024453096.1:c.100023G>C
(TTN)
|
XP_024308864.1:p.Glu33341Asp
|
|
XM_024453097.1:c.97365G>C
(TTN)
|
XP_024308865.1:p.Glu32455Asp
|
|
XM_024453098.1:c.97284G>C
(TTN)
|
XP_024308866.1:p.Glu32428Asp
|
|
XM_024453099.1:c.79047G>C
(TTN)
|
XP_024308867.1:p.Glu26349Asp
|
|
XM_024453100.1:c.68901G>C
(TTN)
|
XP_024308868.1:p.Glu22967Asp
|
|