ENST00000342992.11:c.39591A>T
(TTN)
|
ENSP00000343764.6:p.Val13197=
|
|
ENST00000342175.11:c.20676A>T
(TTN)
|
ENSP00000340554.6:p.Val6892=
|
|
ENST00000359218.10:c.20475A>T
(TTN)
|
ENSP00000352154.5:p.Val6825=
|
|
ENST00000342175.10:c.20676A>T
(TTN)
|
ENSP00000340554.6:p.Val6892=
|
|
ENST00000342992.10:c.39591A>T
(TTN)
|
ENSP00000343764.6:p.Val13197=
|
|
ENST00000359218.9:c.20475A>T
(TTN)
|
ENSP00000352154.5:p.Val6825=
|
|
ENST00000460472.6:c.20100A>T
(TTN)
|
ENSP00000434586.1:p.Val6700=
|
|
ENST00000589042.5:c.47295A>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Val15765=
|
|
ENST00000591111.5:c.42372A>T
(TTN)
|
ENSP00000465570.1:p.Val14124=
|
|
ENST00000615779.4:c.42372A>T
(TTN)
|
ENSP00000483597.1:p.Val14124=
|
|
NM_001256850.1:c.42372A>T
(TTN)
|
NP_001243779.1:p.Val14124=
|
|
NM_001267550.2:c.47295A>T
(TTN)
MANE Select
|
NP_001254479.2:p.Val15765=
|
|
NM_003319.4:c.20100A>T
(TTN)
|
NP_003310.4:p.Val6700=
|
|
NM_133378.4:c.39591A>T
(TTN)
|
NP_596869.4:p.Val13197=
|
|
NM_133432.3:c.20475A>T
(TTN)
|
NP_597676.3:p.Val6825=
|
|
NM_133437.4:c.20676A>T
(TTN)
|
NP_597681.4:p.Val6892=
|
|
NR_038271.1:n.1605-1697T>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.46392A>T
(TTN)
|
XP_011510031.1:p.Val15464=
|
|
XM_011511730.1:c.20286A>T
(TTN)
|
XP_011510032.1:p.Val6762=
|
|
XM_011511731.1:c.20145A>T
(TTN)
|
XP_011510033.1:p.Val6715=
|
|
XM_017004819.1:c.46188A>T
(TTN)
|
XP_016860308.1:p.Val15396=
|
|
XM_017004820.1:c.41586A>T
(TTN)
|
XP_016860309.1:p.Val13862=
|
|
XM_017004821.1:c.41583A>T
(TTN)
|
XP_016860310.1:p.Val13861=
|
|
XM_017004822.1:c.38625A>T
(TTN)
|
XP_016860311.1:p.Val12875=
|
|
XM_017004823.1:c.20241A>T
(TTN)
|
XP_016860312.1:p.Val6747=
|
|
XM_024453094.1:c.41736A>T
(TTN)
|
XP_024308862.1:p.Val13912=
|
|
XM_024453095.1:c.41733A>T
(TTN)
|
XP_024308863.1:p.Val13911=
|
|
XM_024453096.1:c.41166A>T
(TTN)
|
XP_024308864.1:p.Val13722=
|
|
XM_024453097.1:c.38508A>T
(TTN)
|
XP_024308865.1:p.Val12836=
|
|
XM_024453098.1:c.38427A>T
(TTN)
|
XP_024308866.1:p.Val12809=
|
|
XM_024453099.1:c.20190A>T
(TTN)
|
XP_024308867.1:p.Val6730=
|
|
XM_024453100.1:c.10044A>T
(TTN)
|
XP_024308868.1:p.Val3348=
|
|