ENST00000342992.11:c.98309C>A
(TTN)
|
ENSP00000343764.6:p.Ala32770Glu
|
|
ENST00000342175.11:c.79394C>A
(TTN)
|
ENSP00000340554.6:p.Ala26465Glu
|
|
ENST00000359218.10:c.79193C>A
(TTN)
|
ENSP00000352154.5:p.Ala26398Glu
|
|
ENST00000342175.10:c.79394C>A
(TTN)
|
ENSP00000340554.6:p.Ala26465Glu
|
|
ENST00000342992.10:c.98309C>A
(TTN)
|
ENSP00000343764.6:p.Ala32770Glu
|
|
ENST00000359218.9:c.79193C>A
(TTN)
|
ENSP00000352154.5:p.Ala26398Glu
|
|
ENST00000460472.6:c.78818C>A
(TTN)
|
ENSP00000434586.1:p.Ala26273Glu
|
|
ENST00000589042.5:c.106013C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ala35338Glu
|
|
ENST00000591111.5:c.101090C>A
(TTN)
|
ENSP00000465570.1:p.Ala33697Glu
|
|
ENST00000615779.4:c.101090C>A
(TTN)
|
ENSP00000483597.1:p.Ala33697Glu
|
|
NM_001256850.1:c.101090C>A
(TTN)
|
NP_001243779.1:p.Ala33697Glu
|
|
NM_001267550.2:c.106013C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Ala35338Glu
|
|
NM_003319.4:c.78818C>A
(TTN)
|
NP_003310.4:p.Ala26273Glu
|
|
NM_133378.4:c.98309C>A
(TTN)
|
NP_596869.4:p.Ala32770Glu
|
|
NM_133432.3:c.79193C>A
(TTN)
|
NP_597676.3:p.Ala26398Glu
|
|
NM_133437.4:c.79394C>A
(TTN)
|
NP_597681.4:p.Ala26465Glu
|
|
NR_038271.1:n.446+6966G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5130G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.105110C>A
(TTN)
|
XP_011510031.1:p.Ala35037Glu
|
|
XM_011511730.1:c.79004C>A
(TTN)
|
XP_011510032.1:p.Ala26335Glu
|
|
XM_011511731.1:c.78863C>A
(TTN)
|
XP_011510033.1:p.Ala26288Glu
|
|
XM_017004819.1:c.104906C>A
(TTN)
|
XP_016860308.1:p.Ala34969Glu
|
|
XM_017004820.1:c.100304C>A
(TTN)
|
XP_016860309.1:p.Ala33435Glu
|
|
XM_017004821.1:c.100301C>A
(TTN)
|
XP_016860310.1:p.Ala33434Glu
|
|
XM_017004822.1:c.97343C>A
(TTN)
|
XP_016860311.1:p.Ala32448Glu
|
|
XM_017004823.1:c.78959C>A
(TTN)
|
XP_016860312.1:p.Ala26320Glu
|
|
XM_024453094.1:c.100454C>A
(TTN)
|
XP_024308862.1:p.Ala33485Glu
|
|
XM_024453095.1:c.100451C>A
(TTN)
|
XP_024308863.1:p.Ala33484Glu
|
|
XM_024453096.1:c.99884C>A
(TTN)
|
XP_024308864.1:p.Ala33295Glu
|
|
XM_024453097.1:c.97226C>A
(TTN)
|
XP_024308865.1:p.Ala32409Glu
|
|
XM_024453098.1:c.97145C>A
(TTN)
|
XP_024308866.1:p.Ala32382Glu
|
|
XM_024453099.1:c.78908C>A
(TTN)
|
XP_024308867.1:p.Ala26303Glu
|
|
XM_024453100.1:c.68762C>A
(TTN)
|
XP_024308868.1:p.Ala22921Glu
|
|