ENST00000342992.11:c.88206C>T
(TTN)
|
ENSP00000343764.6:p.Phe29402=
|
|
ENST00000342175.11:c.69291C>T
(TTN)
|
ENSP00000340554.6:p.Phe23097=
|
|
ENST00000359218.10:c.69090C>T
(TTN)
|
ENSP00000352154.5:p.Phe23030=
|
|
ENST00000342175.10:c.69291C>T
(TTN)
|
ENSP00000340554.6:p.Phe23097=
|
|
ENST00000342992.10:c.88206C>T
(TTN)
|
ENSP00000343764.6:p.Phe29402=
|
|
ENST00000359218.9:c.69090C>T
(TTN)
|
ENSP00000352154.5:p.Phe23030=
|
|
ENST00000460472.6:c.68715C>T
(TTN)
|
ENSP00000434586.1:p.Phe22905=
|
|
ENST00000589042.5:c.95910C>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Phe31970=
|
|
ENST00000591111.5:c.90987C>T
(TTN)
|
ENSP00000465570.1:p.Phe30329=
|
|
ENST00000615779.4:c.90987C>T
(TTN)
|
ENSP00000483597.1:p.Phe30329=
|
|
NM_001256850.1:c.90987C>T
(TTN)
|
NP_001243779.1:p.Phe30329=
|
|
NM_001267550.2:c.95910C>T
(TTN)
MANE Select
|
NP_001254479.2:p.Phe31970=
|
|
NM_003319.4:c.68715C>T
(TTN)
|
NP_003310.4:p.Phe22905=
|
|
NM_133378.4:c.88206C>T
(TTN)
|
NP_596869.4:p.Phe29402=
|
|
NM_133432.3:c.69090C>T
(TTN)
|
NP_597676.3:p.Phe23030=
|
|
NM_133437.4:c.69291C>T
(TTN)
|
NP_597681.4:p.Phe23097=
|
|
NR_038271.1:n.446+20683G>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+1958G>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.95007C>T
(TTN)
|
XP_011510031.1:p.Phe31669=
|
|
XM_011511730.1:c.68901C>T
(TTN)
|
XP_011510032.1:p.Phe22967=
|
|
XM_011511731.1:c.68760C>T
(TTN)
|
XP_011510033.1:p.Phe22920=
|
|
XM_017004819.1:c.94803C>T
(TTN)
|
XP_016860308.1:p.Phe31601=
|
|
XM_017004820.1:c.90201C>T
(TTN)
|
XP_016860309.1:p.Phe30067=
|
|
XM_017004821.1:c.90198C>T
(TTN)
|
XP_016860310.1:p.Phe30066=
|
|
XM_017004822.1:c.87240C>T
(TTN)
|
XP_016860311.1:p.Phe29080=
|
|
XM_017004823.1:c.68856C>T
(TTN)
|
XP_016860312.1:p.Phe22952=
|
|
XM_024453094.1:c.90351C>T
(TTN)
|
XP_024308862.1:p.Phe30117=
|
|
XM_024453095.1:c.90348C>T
(TTN)
|
XP_024308863.1:p.Phe30116=
|
|
XM_024453096.1:c.89781C>T
(TTN)
|
XP_024308864.1:p.Phe29927=
|
|
XM_024453097.1:c.87123C>T
(TTN)
|
XP_024308865.1:p.Phe29041=
|
|
XM_024453098.1:c.87042C>T
(TTN)
|
XP_024308866.1:p.Phe29014=
|
|
XM_024453099.1:c.68805C>T
(TTN)
|
XP_024308867.1:p.Phe22935=
|
|
XM_024453100.1:c.58659C>T
(TTN)
|
XP_024308868.1:p.Phe19553=
|
|