ENST00000342992.11:c.88221T>C
(TTN)
|
ENSP00000343764.6:p.Leu29407=
|
|
ENST00000342175.11:c.69306T>C
(TTN)
|
ENSP00000340554.6:p.Leu23102=
|
|
ENST00000359218.10:c.69105T>C
(TTN)
|
ENSP00000352154.5:p.Leu23035=
|
|
ENST00000342175.10:c.69306T>C
(TTN)
|
ENSP00000340554.6:p.Leu23102=
|
|
ENST00000342992.10:c.88221T>C
(TTN)
|
ENSP00000343764.6:p.Leu29407=
|
|
ENST00000359218.9:c.69105T>C
(TTN)
|
ENSP00000352154.5:p.Leu23035=
|
|
ENST00000460472.6:c.68730T>C
(TTN)
|
ENSP00000434586.1:p.Leu22910=
|
|
ENST00000589042.5:c.95925T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu31975=
|
|
ENST00000591111.5:c.91002T>C
(TTN)
|
ENSP00000465570.1:p.Leu30334=
|
|
ENST00000615779.4:c.91002T>C
(TTN)
|
ENSP00000483597.1:p.Leu30334=
|
|
NM_001256850.1:c.91002T>C
(TTN)
|
NP_001243779.1:p.Leu30334=
|
|
NM_001267550.2:c.95925T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Leu31975=
|
|
NM_003319.4:c.68730T>C
(TTN)
|
NP_003310.4:p.Leu22910=
|
|
NM_133378.4:c.88221T>C
(TTN)
|
NP_596869.4:p.Leu29407=
|
|
NM_133432.3:c.69105T>C
(TTN)
|
NP_597676.3:p.Leu23035=
|
|
NM_133437.4:c.69306T>C
(TTN)
|
NP_597681.4:p.Leu23102=
|
|
NR_038271.1:n.446+20668A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+1943A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.95022T>C
(TTN)
|
XP_011510031.1:p.Leu31674=
|
|
XM_011511730.1:c.68916T>C
(TTN)
|
XP_011510032.1:p.Leu22972=
|
|
XM_011511731.1:c.68775T>C
(TTN)
|
XP_011510033.1:p.Leu22925=
|
|
XM_017004819.1:c.94818T>C
(TTN)
|
XP_016860308.1:p.Leu31606=
|
|
XM_017004820.1:c.90216T>C
(TTN)
|
XP_016860309.1:p.Leu30072=
|
|
XM_017004821.1:c.90213T>C
(TTN)
|
XP_016860310.1:p.Leu30071=
|
|
XM_017004822.1:c.87255T>C
(TTN)
|
XP_016860311.1:p.Leu29085=
|
|
XM_017004823.1:c.68871T>C
(TTN)
|
XP_016860312.1:p.Leu22957=
|
|
XM_024453094.1:c.90366T>C
(TTN)
|
XP_024308862.1:p.Leu30122=
|
|
XM_024453095.1:c.90363T>C
(TTN)
|
XP_024308863.1:p.Leu30121=
|
|
XM_024453096.1:c.89796T>C
(TTN)
|
XP_024308864.1:p.Leu29932=
|
|
XM_024453097.1:c.87138T>C
(TTN)
|
XP_024308865.1:p.Leu29046=
|
|
XM_024453098.1:c.87057T>C
(TTN)
|
XP_024308866.1:p.Leu29019=
|
|
XM_024453099.1:c.68820T>C
(TTN)
|
XP_024308867.1:p.Leu22940=
|
|
XM_024453100.1:c.58674T>C
(TTN)
|
XP_024308868.1:p.Leu19558=
|
|