ENST00000342992.11:c.98469A>G
(TTN)
|
ENSP00000343764.6:p.Glu32823=
|
|
ENST00000342175.11:c.79554A>G
(TTN)
|
ENSP00000340554.6:p.Glu26518=
|
|
ENST00000359218.10:c.79353A>G
(TTN)
|
ENSP00000352154.5:p.Glu26451=
|
|
ENST00000342175.10:c.79554A>G
(TTN)
|
ENSP00000340554.6:p.Glu26518=
|
|
ENST00000342992.10:c.98469A>G
(TTN)
|
ENSP00000343764.6:p.Glu32823=
|
|
ENST00000359218.9:c.79353A>G
(TTN)
|
ENSP00000352154.5:p.Glu26451=
|
|
ENST00000460472.6:c.78978A>G
(TTN)
|
ENSP00000434586.1:p.Glu26326=
|
|
ENST00000589042.5:c.106173A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu35391=
|
|
ENST00000591111.5:c.101250A>G
(TTN)
|
ENSP00000465570.1:p.Glu33750=
|
|
ENST00000615779.4:c.101250A>G
(TTN)
|
ENSP00000483597.1:p.Glu33750=
|
|
NM_001256850.1:c.101250A>G
(TTN)
|
NP_001243779.1:p.Glu33750=
|
|
NM_001267550.2:c.106173A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Glu35391=
|
|
NM_003319.4:c.78978A>G
(TTN)
|
NP_003310.4:p.Glu26326=
|
|
NM_133378.4:c.98469A>G
(TTN)
|
NP_596869.4:p.Glu32823=
|
|
NM_133432.3:c.79353A>G
(TTN)
|
NP_597676.3:p.Glu26451=
|
|
NM_133437.4:c.79554A>G
(TTN)
|
NP_597681.4:p.Glu26518=
|
|
NR_038271.1:n.446+6806T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5290T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.105270A>G
(TTN)
|
XP_011510031.1:p.Glu35090=
|
|
XM_011511730.1:c.79164A>G
(TTN)
|
XP_011510032.1:p.Glu26388=
|
|
XM_011511731.1:c.79023A>G
(TTN)
|
XP_011510033.1:p.Glu26341=
|
|
XM_017004819.1:c.105066A>G
(TTN)
|
XP_016860308.1:p.Glu35022=
|
|
XM_017004820.1:c.100464A>G
(TTN)
|
XP_016860309.1:p.Glu33488=
|
|
XM_017004821.1:c.100461A>G
(TTN)
|
XP_016860310.1:p.Glu33487=
|
|
XM_017004822.1:c.97503A>G
(TTN)
|
XP_016860311.1:p.Glu32501=
|
|
XM_017004823.1:c.79119A>G
(TTN)
|
XP_016860312.1:p.Glu26373=
|
|
XM_024453094.1:c.100614A>G
(TTN)
|
XP_024308862.1:p.Glu33538=
|
|
XM_024453095.1:c.100611A>G
(TTN)
|
XP_024308863.1:p.Glu33537=
|
|
XM_024453096.1:c.100044A>G
(TTN)
|
XP_024308864.1:p.Glu33348=
|
|
XM_024453097.1:c.97386A>G
(TTN)
|
XP_024308865.1:p.Glu32462=
|
|
XM_024453098.1:c.97305A>G
(TTN)
|
XP_024308866.1:p.Glu32435=
|
|
XM_024453099.1:c.79068A>G
(TTN)
|
XP_024308867.1:p.Glu26356=
|
|
XM_024453100.1:c.68922A>G
(TTN)
|
XP_024308868.1:p.Glu22974=
|
|