ENST00000342992.11:c.98415A>C
(TTN)
|
ENSP00000343764.6:p.Gln32805His
|
|
ENST00000342175.11:c.79500A>C
(TTN)
|
ENSP00000340554.6:p.Gln26500His
|
|
ENST00000359218.10:c.79299A>C
(TTN)
|
ENSP00000352154.5:p.Gln26433His
|
|
ENST00000342175.10:c.79500A>C
(TTN)
|
ENSP00000340554.6:p.Gln26500His
|
|
ENST00000342992.10:c.98415A>C
(TTN)
|
ENSP00000343764.6:p.Gln32805His
|
|
ENST00000359218.9:c.79299A>C
(TTN)
|
ENSP00000352154.5:p.Gln26433His
|
|
ENST00000460472.6:c.78924A>C
(TTN)
|
ENSP00000434586.1:p.Gln26308His
|
|
ENST00000589042.5:c.106119A>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gln35373His
|
|
ENST00000591111.5:c.101196A>C
(TTN)
|
ENSP00000465570.1:p.Gln33732His
|
|
ENST00000615779.4:c.101196A>C
(TTN)
|
ENSP00000483597.1:p.Gln33732His
|
|
NM_001256850.1:c.101196A>C
(TTN)
|
NP_001243779.1:p.Gln33732His
|
|
NM_001267550.2:c.106119A>C
(TTN)
MANE Select
|
NP_001254479.2:p.Gln35373His
|
|
NM_003319.4:c.78924A>C
(TTN)
|
NP_003310.4:p.Gln26308His
|
|
NM_133378.4:c.98415A>C
(TTN)
|
NP_596869.4:p.Gln32805His
|
|
NM_133432.3:c.79299A>C
(TTN)
|
NP_597676.3:p.Gln26433His
|
|
NM_133437.4:c.79500A>C
(TTN)
|
NP_597681.4:p.Gln26500His
|
|
NR_038271.1:n.446+6860T>G
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5236T>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.105216A>C
(TTN)
|
XP_011510031.1:p.Gln35072His
|
|
XM_011511730.1:c.79110A>C
(TTN)
|
XP_011510032.1:p.Gln26370His
|
|
XM_011511731.1:c.78969A>C
(TTN)
|
XP_011510033.1:p.Gln26323His
|
|
XM_017004819.1:c.105012A>C
(TTN)
|
XP_016860308.1:p.Gln35004His
|
|
XM_017004820.1:c.100410A>C
(TTN)
|
XP_016860309.1:p.Gln33470His
|
|
XM_017004821.1:c.100407A>C
(TTN)
|
XP_016860310.1:p.Gln33469His
|
|
XM_017004822.1:c.97449A>C
(TTN)
|
XP_016860311.1:p.Gln32483His
|
|
XM_017004823.1:c.79065A>C
(TTN)
|
XP_016860312.1:p.Gln26355His
|
|
XM_024453094.1:c.100560A>C
(TTN)
|
XP_024308862.1:p.Gln33520His
|
|
XM_024453095.1:c.100557A>C
(TTN)
|
XP_024308863.1:p.Gln33519His
|
|
XM_024453096.1:c.99990A>C
(TTN)
|
XP_024308864.1:p.Gln33330His
|
|
XM_024453097.1:c.97332A>C
(TTN)
|
XP_024308865.1:p.Gln32444His
|
|
XM_024453098.1:c.97251A>C
(TTN)
|
XP_024308866.1:p.Gln32417His
|
|
XM_024453099.1:c.79014A>C
(TTN)
|
XP_024308867.1:p.Gln26338His
|
|
XM_024453100.1:c.68868A>C
(TTN)
|
XP_024308868.1:p.Gln22956His
|
|