ENST00000342992.11:c.69579A>G
(TTN)
|
ENSP00000343764.6:p.Leu23193=
|
|
ENST00000342175.11:c.50664A>G
(TTN)
|
ENSP00000340554.6:p.Leu16888=
|
|
ENST00000359218.10:c.50463A>G
(TTN)
|
ENSP00000352154.5:p.Leu16821=
|
|
ENST00000342175.10:c.50664A>G
(TTN)
|
ENSP00000340554.6:p.Leu16888=
|
|
ENST00000342992.10:c.69579A>G
(TTN)
|
ENSP00000343764.6:p.Leu23193=
|
|
ENST00000359218.9:c.50463A>G
(TTN)
|
ENSP00000352154.5:p.Leu16821=
|
|
ENST00000460472.6:c.50088A>G
(TTN)
|
ENSP00000434586.1:p.Leu16696=
|
|
ENST00000589042.5:c.77283A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu25761=
|
|
ENST00000591111.5:c.72360A>G
(TTN)
|
ENSP00000465570.1:p.Leu24120=
|
|
ENST00000615779.4:c.72360A>G
(TTN)
|
ENSP00000483597.1:p.Leu24120=
|
|
NM_001256850.1:c.72360A>G
(TTN)
|
NP_001243779.1:p.Leu24120=
|
|
NM_001267550.2:c.77283A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Leu25761=
|
|
NM_003319.4:c.50088A>G
(TTN)
|
NP_003310.4:p.Leu16696=
|
|
NM_133378.4:c.69579A>G
(TTN)
|
NP_596869.4:p.Leu23193=
|
|
NM_133432.3:c.50463A>G
(TTN)
|
NP_597676.3:p.Leu16821=
|
|
NM_133437.4:c.50664A>G
(TTN)
|
NP_597681.4:p.Leu16888=
|
|
NR_038271.1:n.447-2451T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-13723T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.76380A>G
(TTN)
|
XP_011510031.1:p.Leu25460=
|
|
XM_011511730.1:c.50274A>G
(TTN)
|
XP_011510032.1:p.Leu16758=
|
|
XM_011511731.1:c.50133A>G
(TTN)
|
XP_011510033.1:p.Leu16711=
|
|
XM_017004819.1:c.76176A>G
(TTN)
|
XP_016860308.1:p.Leu25392=
|
|
XM_017004820.1:c.71574A>G
(TTN)
|
XP_016860309.1:p.Leu23858=
|
|
XM_017004821.1:c.71571A>G
(TTN)
|
XP_016860310.1:p.Leu23857=
|
|
XM_017004822.1:c.68613A>G
(TTN)
|
XP_016860311.1:p.Leu22871=
|
|
XM_017004823.1:c.50229A>G
(TTN)
|
XP_016860312.1:p.Leu16743=
|
|
XM_024453094.1:c.71724A>G
(TTN)
|
XP_024308862.1:p.Leu23908=
|
|
XM_024453095.1:c.71721A>G
(TTN)
|
XP_024308863.1:p.Leu23907=
|
|
XM_024453096.1:c.71154A>G
(TTN)
|
XP_024308864.1:p.Leu23718=
|
|
XM_024453097.1:c.68496A>G
(TTN)
|
XP_024308865.1:p.Leu22832=
|
|
XM_024453098.1:c.68415A>G
(TTN)
|
XP_024308866.1:p.Leu22805=
|
|
XM_024453099.1:c.50178A>G
(TTN)
|
XP_024308867.1:p.Leu16726=
|
|
XM_024453100.1:c.40032A>G
(TTN)
|
XP_024308868.1:p.Leu13344=
|
|