ENST00000342992.11:c.91872A>T
(TTN)
|
ENSP00000343764.6:p.Ala30624=
|
|
ENST00000342175.11:c.72957A>T
(TTN)
|
ENSP00000340554.6:p.Ala24319=
|
|
ENST00000359218.10:c.72756A>T
(TTN)
|
ENSP00000352154.5:p.Ala24252=
|
|
ENST00000342175.10:c.72957A>T
(TTN)
|
ENSP00000340554.6:p.Ala24319=
|
|
ENST00000342992.10:c.91872A>T
(TTN)
|
ENSP00000343764.6:p.Ala30624=
|
|
ENST00000359218.9:c.72756A>T
(TTN)
|
ENSP00000352154.5:p.Ala24252=
|
|
ENST00000460472.6:c.72381A>T
(TTN)
|
ENSP00000434586.1:p.Ala24127=
|
|
ENST00000589042.5:c.99576A>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ala33192=
|
|
ENST00000591111.5:c.94653A>T
(TTN)
|
ENSP00000465570.1:p.Ala31551=
|
|
ENST00000615779.4:c.94653A>T
(TTN)
|
ENSP00000483597.1:p.Ala31551=
|
|
NM_001256850.1:c.94653A>T
(TTN)
|
NP_001243779.1:p.Ala31551=
|
|
NM_001267550.2:c.99576A>T
(TTN)
MANE Select
|
NP_001254479.2:p.Ala33192=
|
|
NM_003319.4:c.72381A>T
(TTN)
|
NP_003310.4:p.Ala24127=
|
|
NM_133378.4:c.91872A>T
(TTN)
|
NP_596869.4:p.Ala30624=
|
|
NM_133432.3:c.72756A>T
(TTN)
|
NP_597676.3:p.Ala24252=
|
|
NM_133437.4:c.72957A>T
(TTN)
|
NP_597681.4:p.Ala24319=
|
|
NR_038271.1:n.446+13995T>A
(TTN-AS1)
|
|
|
NR_038272.1:n.587T>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.98673A>T
(TTN)
|
XP_011510031.1:p.Ala32891=
|
|
XM_011511730.1:c.72567A>T
(TTN)
|
XP_011510032.1:p.Ala24189=
|
|
XM_011511731.1:c.72426A>T
(TTN)
|
XP_011510033.1:p.Ala24142=
|
|
XM_017004819.1:c.98469A>T
(TTN)
|
XP_016860308.1:p.Ala32823=
|
|
XM_017004820.1:c.93867A>T
(TTN)
|
XP_016860309.1:p.Ala31289=
|
|
XM_017004821.1:c.93864A>T
(TTN)
|
XP_016860310.1:p.Ala31288=
|
|
XM_017004822.1:c.90906A>T
(TTN)
|
XP_016860311.1:p.Ala30302=
|
|
XM_017004823.1:c.72522A>T
(TTN)
|
XP_016860312.1:p.Ala24174=
|
|
XM_024453094.1:c.94017A>T
(TTN)
|
XP_024308862.1:p.Ala31339=
|
|
XM_024453095.1:c.94014A>T
(TTN)
|
XP_024308863.1:p.Ala31338=
|
|
XM_024453096.1:c.93447A>T
(TTN)
|
XP_024308864.1:p.Ala31149=
|
|
XM_024453097.1:c.90789A>T
(TTN)
|
XP_024308865.1:p.Ala30263=
|
|
XM_024453098.1:c.90708A>T
(TTN)
|
XP_024308866.1:p.Ala30236=
|
|
XM_024453099.1:c.72471A>T
(TTN)
|
XP_024308867.1:p.Ala24157=
|
|
XM_024453100.1:c.62325A>T
(TTN)
|
XP_024308868.1:p.Ala20775=
|
|