ENST00000342992.11:c.91866G>A
(TTN)
|
ENSP00000343764.6:p.Leu30622=
|
|
ENST00000342175.11:c.72951G>A
(TTN)
|
ENSP00000340554.6:p.Leu24317=
|
|
ENST00000359218.10:c.72750G>A
(TTN)
|
ENSP00000352154.5:p.Leu24250=
|
|
ENST00000342175.10:c.72951G>A
(TTN)
|
ENSP00000340554.6:p.Leu24317=
|
|
ENST00000342992.10:c.91866G>A
(TTN)
|
ENSP00000343764.6:p.Leu30622=
|
|
ENST00000359218.9:c.72750G>A
(TTN)
|
ENSP00000352154.5:p.Leu24250=
|
|
ENST00000460472.6:c.72375G>A
(TTN)
|
ENSP00000434586.1:p.Leu24125=
|
|
ENST00000589042.5:c.99570G>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu33190=
|
|
ENST00000591111.5:c.94647G>A
(TTN)
|
ENSP00000465570.1:p.Leu31549=
|
|
ENST00000615779.4:c.94647G>A
(TTN)
|
ENSP00000483597.1:p.Leu31549=
|
|
NM_001256850.1:c.94647G>A
(TTN)
|
NP_001243779.1:p.Leu31549=
|
|
NM_001267550.2:c.99570G>A
(TTN)
MANE Select
|
NP_001254479.2:p.Leu33190=
|
|
NM_003319.4:c.72375G>A
(TTN)
|
NP_003310.4:p.Leu24125=
|
|
NM_133378.4:c.91866G>A
(TTN)
|
NP_596869.4:p.Leu30622=
|
|
NM_133432.3:c.72750G>A
(TTN)
|
NP_597676.3:p.Leu24250=
|
|
NM_133437.4:c.72951G>A
(TTN)
|
NP_597681.4:p.Leu24317=
|
|
NR_038271.1:n.446+14001C>T
(TTN-AS1)
|
|
|
NR_038272.1:n.593C>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.98667G>A
(TTN)
|
XP_011510031.1:p.Leu32889=
|
|
XM_011511730.1:c.72561G>A
(TTN)
|
XP_011510032.1:p.Leu24187=
|
|
XM_011511731.1:c.72420G>A
(TTN)
|
XP_011510033.1:p.Leu24140=
|
|
XM_017004819.1:c.98463G>A
(TTN)
|
XP_016860308.1:p.Leu32821=
|
|
XM_017004820.1:c.93861G>A
(TTN)
|
XP_016860309.1:p.Leu31287=
|
|
XM_017004821.1:c.93858G>A
(TTN)
|
XP_016860310.1:p.Leu31286=
|
|
XM_017004822.1:c.90900G>A
(TTN)
|
XP_016860311.1:p.Leu30300=
|
|
XM_017004823.1:c.72516G>A
(TTN)
|
XP_016860312.1:p.Leu24172=
|
|
XM_024453094.1:c.94011G>A
(TTN)
|
XP_024308862.1:p.Leu31337=
|
|
XM_024453095.1:c.94008G>A
(TTN)
|
XP_024308863.1:p.Leu31336=
|
|
XM_024453096.1:c.93441G>A
(TTN)
|
XP_024308864.1:p.Leu31147=
|
|
XM_024453097.1:c.90783G>A
(TTN)
|
XP_024308865.1:p.Leu30261=
|
|
XM_024453098.1:c.90702G>A
(TTN)
|
XP_024308866.1:p.Leu30234=
|
|
XM_024453099.1:c.72465G>A
(TTN)
|
XP_024308867.1:p.Leu24155=
|
|
XM_024453100.1:c.62319G>A
(TTN)
|
XP_024308868.1:p.Leu20773=
|
|