ENST00000342992.11:c.57243A>T
(TTN)
|
ENSP00000343764.6:p.Pro19081=
|
|
ENST00000342175.11:c.38328A>T
(TTN)
|
ENSP00000340554.6:p.Pro12776=
|
|
ENST00000359218.10:c.38127A>T
(TTN)
|
ENSP00000352154.5:p.Pro12709=
|
|
ENST00000342175.10:c.38328A>T
(TTN)
|
ENSP00000340554.6:p.Pro12776=
|
|
ENST00000342992.10:c.57243A>T
(TTN)
|
ENSP00000343764.6:p.Pro19081=
|
|
ENST00000359218.9:c.38127A>T
(TTN)
|
ENSP00000352154.5:p.Pro12709=
|
|
ENST00000460472.6:c.37752A>T
(TTN)
|
ENSP00000434586.1:p.Pro12584=
|
|
ENST00000589042.5:c.64947A>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Pro21649=
|
|
ENST00000591111.5:c.60024A>T
(TTN)
|
ENSP00000465570.1:p.Pro20008=
|
|
ENST00000615779.4:c.60024A>T
(TTN)
|
ENSP00000483597.1:p.Pro20008=
|
|
NM_001256850.1:c.60024A>T
(TTN)
|
NP_001243779.1:p.Pro20008=
|
|
NM_001267550.2:c.64947A>T
(TTN)
MANE Select
|
NP_001254479.2:p.Pro21649=
|
|
NM_003319.4:c.37752A>T
(TTN)
|
NP_003310.4:p.Pro12584=
|
|
NM_133378.4:c.57243A>T
(TTN)
|
NP_596869.4:p.Pro19081=
|
|
NM_133432.3:c.38127A>T
(TTN)
|
NP_597676.3:p.Pro12709=
|
|
NM_133437.4:c.38328A>T
(TTN)
|
NP_597681.4:p.Pro12776=
|
|
NR_038271.1:n.597-12902T>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2889T>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.64044A>T
(TTN)
|
XP_011510031.1:p.Pro21348=
|
|
XM_011511730.1:c.37938A>T
(TTN)
|
XP_011510032.1:p.Pro12646=
|
|
XM_011511731.1:c.37797A>T
(TTN)
|
XP_011510033.1:p.Pro12599=
|
|
XM_017004819.1:c.63840A>T
(TTN)
|
XP_016860308.1:p.Pro21280=
|
|
XM_017004820.1:c.59238A>T
(TTN)
|
XP_016860309.1:p.Pro19746=
|
|
XM_017004821.1:c.59235A>T
(TTN)
|
XP_016860310.1:p.Pro19745=
|
|
XM_017004822.1:c.56277A>T
(TTN)
|
XP_016860311.1:p.Pro18759=
|
|
XM_017004823.1:c.37893A>T
(TTN)
|
XP_016860312.1:p.Pro12631=
|
|
XM_024453094.1:c.59388A>T
(TTN)
|
XP_024308862.1:p.Pro19796=
|
|
XM_024453095.1:c.59385A>T
(TTN)
|
XP_024308863.1:p.Pro19795=
|
|
XM_024453096.1:c.58818A>T
(TTN)
|
XP_024308864.1:p.Pro19606=
|
|
XM_024453097.1:c.56160A>T
(TTN)
|
XP_024308865.1:p.Pro18720=
|
|
XM_024453098.1:c.56079A>T
(TTN)
|
XP_024308866.1:p.Pro18693=
|
|
XM_024453099.1:c.37842A>T
(TTN)
|
XP_024308867.1:p.Pro12614=
|
|
XM_024453100.1:c.27696A>T
(TTN)
|
XP_024308868.1:p.Pro9232=
|
|