ENST00000342992.11:c.98498A>G
(TTN)
|
ENSP00000343764.6:p.Glu32833Gly
|
|
ENST00000342175.11:c.79583A>G
(TTN)
|
ENSP00000340554.6:p.Glu26528Gly
|
|
ENST00000359218.10:c.79382A>G
(TTN)
|
ENSP00000352154.5:p.Glu26461Gly
|
|
ENST00000342175.10:c.79583A>G
(TTN)
|
ENSP00000340554.6:p.Glu26528Gly
|
|
ENST00000342992.10:c.98498A>G
(TTN)
|
ENSP00000343764.6:p.Glu32833Gly
|
|
ENST00000359218.9:c.79382A>G
(TTN)
|
ENSP00000352154.5:p.Glu26461Gly
|
|
ENST00000460472.6:c.79007A>G
(TTN)
|
ENSP00000434586.1:p.Glu26336Gly
|
|
ENST00000589042.5:c.106202A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu35401Gly
|
|
ENST00000591111.5:c.101279A>G
(TTN)
|
ENSP00000465570.1:p.Glu33760Gly
|
|
ENST00000615779.4:c.101279A>G
(TTN)
|
ENSP00000483597.1:p.Glu33760Gly
|
|
NM_001256850.1:c.101279A>G
(TTN)
|
NP_001243779.1:p.Glu33760Gly
|
|
NM_001267550.2:c.106202A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Glu35401Gly
|
|
NM_003319.4:c.79007A>G
(TTN)
|
NP_003310.4:p.Glu26336Gly
|
|
NM_133378.4:c.98498A>G
(TTN)
|
NP_596869.4:p.Glu32833Gly
|
|
NM_133432.3:c.79382A>G
(TTN)
|
NP_597676.3:p.Glu26461Gly
|
|
NM_133437.4:c.79583A>G
(TTN)
|
NP_597681.4:p.Glu26528Gly
|
|
NR_038271.1:n.446+6777T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5319T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.105299A>G
(TTN)
|
XP_011510031.1:p.Glu35100Gly
|
|
XM_011511730.1:c.79193A>G
(TTN)
|
XP_011510032.1:p.Glu26398Gly
|
|
XM_011511731.1:c.79052A>G
(TTN)
|
XP_011510033.1:p.Glu26351Gly
|
|
XM_017004819.1:c.105095A>G
(TTN)
|
XP_016860308.1:p.Glu35032Gly
|
|
XM_017004820.1:c.100493A>G
(TTN)
|
XP_016860309.1:p.Glu33498Gly
|
|
XM_017004821.1:c.100490A>G
(TTN)
|
XP_016860310.1:p.Glu33497Gly
|
|
XM_017004822.1:c.97532A>G
(TTN)
|
XP_016860311.1:p.Glu32511Gly
|
|
XM_017004823.1:c.79148A>G
(TTN)
|
XP_016860312.1:p.Glu26383Gly
|
|
XM_024453094.1:c.100643A>G
(TTN)
|
XP_024308862.1:p.Glu33548Gly
|
|
XM_024453095.1:c.100640A>G
(TTN)
|
XP_024308863.1:p.Glu33547Gly
|
|
XM_024453096.1:c.100073A>G
(TTN)
|
XP_024308864.1:p.Glu33358Gly
|
|
XM_024453097.1:c.97415A>G
(TTN)
|
XP_024308865.1:p.Glu32472Gly
|
|
XM_024453098.1:c.97334A>G
(TTN)
|
XP_024308866.1:p.Glu32445Gly
|
|
XM_024453099.1:c.79097A>G
(TTN)
|
XP_024308867.1:p.Glu26366Gly
|
|
XM_024453100.1:c.68951A>G
(TTN)
|
XP_024308868.1:p.Glu22984Gly
|
|