ENST00000342992.11:c.69600T>C
(TTN)
|
ENSP00000343764.6:p.Leu23200=
|
|
ENST00000342175.11:c.50685T>C
(TTN)
|
ENSP00000340554.6:p.Leu16895=
|
|
ENST00000359218.10:c.50484T>C
(TTN)
|
ENSP00000352154.5:p.Leu16828=
|
|
ENST00000342175.10:c.50685T>C
(TTN)
|
ENSP00000340554.6:p.Leu16895=
|
|
ENST00000342992.10:c.69600T>C
(TTN)
|
ENSP00000343764.6:p.Leu23200=
|
|
ENST00000359218.9:c.50484T>C
(TTN)
|
ENSP00000352154.5:p.Leu16828=
|
|
ENST00000460472.6:c.50109T>C
(TTN)
|
ENSP00000434586.1:p.Leu16703=
|
|
ENST00000589042.5:c.77304T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu25768=
|
|
ENST00000591111.5:c.72381T>C
(TTN)
|
ENSP00000465570.1:p.Leu24127=
|
|
ENST00000615779.4:c.72381T>C
(TTN)
|
ENSP00000483597.1:p.Leu24127=
|
|
NM_001256850.1:c.72381T>C
(TTN)
|
NP_001243779.1:p.Leu24127=
|
|
NM_001267550.2:c.77304T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Leu25768=
|
|
NM_003319.4:c.50109T>C
(TTN)
|
NP_003310.4:p.Leu16703=
|
|
NM_133378.4:c.69600T>C
(TTN)
|
NP_596869.4:p.Leu23200=
|
|
NM_133432.3:c.50484T>C
(TTN)
|
NP_597676.3:p.Leu16828=
|
|
NM_133437.4:c.50685T>C
(TTN)
|
NP_597681.4:p.Leu16895=
|
|
NR_038271.1:n.447-2472A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-13744A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.76401T>C
(TTN)
|
XP_011510031.1:p.Leu25467=
|
|
XM_011511730.1:c.50295T>C
(TTN)
|
XP_011510032.1:p.Leu16765=
|
|
XM_011511731.1:c.50154T>C
(TTN)
|
XP_011510033.1:p.Leu16718=
|
|
XM_017004819.1:c.76197T>C
(TTN)
|
XP_016860308.1:p.Leu25399=
|
|
XM_017004820.1:c.71595T>C
(TTN)
|
XP_016860309.1:p.Leu23865=
|
|
XM_017004821.1:c.71592T>C
(TTN)
|
XP_016860310.1:p.Leu23864=
|
|
XM_017004822.1:c.68634T>C
(TTN)
|
XP_016860311.1:p.Leu22878=
|
|
XM_017004823.1:c.50250T>C
(TTN)
|
XP_016860312.1:p.Leu16750=
|
|
XM_024453094.1:c.71745T>C
(TTN)
|
XP_024308862.1:p.Leu23915=
|
|
XM_024453095.1:c.71742T>C
(TTN)
|
XP_024308863.1:p.Leu23914=
|
|
XM_024453096.1:c.71175T>C
(TTN)
|
XP_024308864.1:p.Leu23725=
|
|
XM_024453097.1:c.68517T>C
(TTN)
|
XP_024308865.1:p.Leu22839=
|
|
XM_024453098.1:c.68436T>C
(TTN)
|
XP_024308866.1:p.Leu22812=
|
|
XM_024453099.1:c.50199T>C
(TTN)
|
XP_024308867.1:p.Leu16733=
|
|
XM_024453100.1:c.40053T>C
(TTN)
|
XP_024308868.1:p.Leu13351=
|
|