ENST00000342992.11:c.57266T>A
(TTN)
|
ENSP00000343764.6:p.Phe19089Tyr
|
|
ENST00000342175.11:c.38351T>A
(TTN)
|
ENSP00000340554.6:p.Phe12784Tyr
|
|
ENST00000359218.10:c.38150T>A
(TTN)
|
ENSP00000352154.5:p.Phe12717Tyr
|
|
ENST00000342175.10:c.38351T>A
(TTN)
|
ENSP00000340554.6:p.Phe12784Tyr
|
|
ENST00000342992.10:c.57266T>A
(TTN)
|
ENSP00000343764.6:p.Phe19089Tyr
|
|
ENST00000359218.9:c.38150T>A
(TTN)
|
ENSP00000352154.5:p.Phe12717Tyr
|
|
ENST00000460472.6:c.37775T>A
(TTN)
|
ENSP00000434586.1:p.Phe12592Tyr
|
|
ENST00000589042.5:c.64970T>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Phe21657Tyr
|
|
ENST00000591111.5:c.60047T>A
(TTN)
|
ENSP00000465570.1:p.Phe20016Tyr
|
|
ENST00000615779.4:c.60047T>A
(TTN)
|
ENSP00000483597.1:p.Phe20016Tyr
|
|
NM_001256850.1:c.60047T>A
(TTN)
|
NP_001243779.1:p.Phe20016Tyr
|
|
NM_001267550.2:c.64970T>A
(TTN)
MANE Select
|
NP_001254479.2:p.Phe21657Tyr
|
|
NM_003319.4:c.37775T>A
(TTN)
|
NP_003310.4:p.Phe12592Tyr
|
|
NM_133378.4:c.57266T>A
(TTN)
|
NP_596869.4:p.Phe19089Tyr
|
|
NM_133432.3:c.38150T>A
(TTN)
|
NP_597676.3:p.Phe12717Tyr
|
|
NM_133437.4:c.38351T>A
(TTN)
|
NP_597681.4:p.Phe12784Tyr
|
|
NR_038271.1:n.597-12925A>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2866A>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.64067T>A
(TTN)
|
XP_011510031.1:p.Phe21356Tyr
|
|
XM_011511730.1:c.37961T>A
(TTN)
|
XP_011510032.1:p.Phe12654Tyr
|
|
XM_011511731.1:c.37820T>A
(TTN)
|
XP_011510033.1:p.Phe12607Tyr
|
|
XM_017004819.1:c.63863T>A
(TTN)
|
XP_016860308.1:p.Phe21288Tyr
|
|
XM_017004820.1:c.59261T>A
(TTN)
|
XP_016860309.1:p.Phe19754Tyr
|
|
XM_017004821.1:c.59258T>A
(TTN)
|
XP_016860310.1:p.Phe19753Tyr
|
|
XM_017004822.1:c.56300T>A
(TTN)
|
XP_016860311.1:p.Phe18767Tyr
|
|
XM_017004823.1:c.37916T>A
(TTN)
|
XP_016860312.1:p.Phe12639Tyr
|
|
XM_024453094.1:c.59411T>A
(TTN)
|
XP_024308862.1:p.Phe19804Tyr
|
|
XM_024453095.1:c.59408T>A
(TTN)
|
XP_024308863.1:p.Phe19803Tyr
|
|
XM_024453096.1:c.58841T>A
(TTN)
|
XP_024308864.1:p.Phe19614Tyr
|
|
XM_024453097.1:c.56183T>A
(TTN)
|
XP_024308865.1:p.Phe18728Tyr
|
|
XM_024453098.1:c.56102T>A
(TTN)
|
XP_024308866.1:p.Phe18701Tyr
|
|
XM_024453099.1:c.37865T>A
(TTN)
|
XP_024308867.1:p.Phe12622Tyr
|
|
XM_024453100.1:c.27719T>A
(TTN)
|
XP_024308868.1:p.Phe9240Tyr
|
|