ENST00000342992.11:c.39531A>G
(TTN)
|
ENSP00000343764.6:p.Glu13177=
|
|
ENST00000342175.11:c.20616A>G
(TTN)
|
ENSP00000340554.6:p.Glu6872=
|
|
ENST00000359218.10:c.20415A>G
(TTN)
|
ENSP00000352154.5:p.Glu6805=
|
|
ENST00000342175.10:c.20616A>G
(TTN)
|
ENSP00000340554.6:p.Glu6872=
|
|
ENST00000342992.10:c.39531A>G
(TTN)
|
ENSP00000343764.6:p.Glu13177=
|
|
ENST00000359218.9:c.20415A>G
(TTN)
|
ENSP00000352154.5:p.Glu6805=
|
|
ENST00000460472.6:c.20040A>G
(TTN)
|
ENSP00000434586.1:p.Glu6680=
|
|
ENST00000589042.5:c.47235A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu15745=
|
|
ENST00000591111.5:c.42312A>G
(TTN)
|
ENSP00000465570.1:p.Glu14104=
|
|
ENST00000615779.4:c.42312A>G
(TTN)
|
ENSP00000483597.1:p.Glu14104=
|
|
NM_001256850.1:c.42312A>G
(TTN)
|
NP_001243779.1:p.Glu14104=
|
|
NM_001267550.2:c.47235A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Glu15745=
|
|
NM_003319.4:c.20040A>G
(TTN)
|
NP_003310.4:p.Glu6680=
|
|
NM_133378.4:c.39531A>G
(TTN)
|
NP_596869.4:p.Glu13177=
|
|
NM_133432.3:c.20415A>G
(TTN)
|
NP_597676.3:p.Glu6805=
|
|
NM_133437.4:c.20616A>G
(TTN)
|
NP_597681.4:p.Glu6872=
|
|
NR_038271.1:n.1605-1530T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.46332A>G
(TTN)
|
XP_011510031.1:p.Glu15444=
|
|
XM_011511730.1:c.20226A>G
(TTN)
|
XP_011510032.1:p.Glu6742=
|
|
XM_011511731.1:c.20085A>G
(TTN)
|
XP_011510033.1:p.Glu6695=
|
|
XM_017004819.1:c.46128A>G
(TTN)
|
XP_016860308.1:p.Glu15376=
|
|
XM_017004820.1:c.41526A>G
(TTN)
|
XP_016860309.1:p.Glu13842=
|
|
XM_017004821.1:c.41523A>G
(TTN)
|
XP_016860310.1:p.Glu13841=
|
|
XM_017004822.1:c.38565A>G
(TTN)
|
XP_016860311.1:p.Glu12855=
|
|
XM_017004823.1:c.20181A>G
(TTN)
|
XP_016860312.1:p.Glu6727=
|
|
XM_024453094.1:c.41676A>G
(TTN)
|
XP_024308862.1:p.Glu13892=
|
|
XM_024453095.1:c.41673A>G
(TTN)
|
XP_024308863.1:p.Glu13891=
|
|
XM_024453096.1:c.41106A>G
(TTN)
|
XP_024308864.1:p.Glu13702=
|
|
XM_024453097.1:c.38448A>G
(TTN)
|
XP_024308865.1:p.Glu12816=
|
|
XM_024453098.1:c.38367A>G
(TTN)
|
XP_024308866.1:p.Glu12789=
|
|
XM_024453099.1:c.20130A>G
(TTN)
|
XP_024308867.1:p.Glu6710=
|
|
XM_024453100.1:c.9984A>G
(TTN)
|
XP_024308868.1:p.Glu3328=
|
|