ENST00000342992.11:c.92339T>G
(TTN)
|
ENSP00000343764.6:p.Val30780Gly
|
|
ENST00000342175.11:c.73424T>G
(TTN)
|
ENSP00000340554.6:p.Val24475Gly
|
|
ENST00000359218.10:c.73223T>G
(TTN)
|
ENSP00000352154.5:p.Val24408Gly
|
|
ENST00000342175.10:c.73424T>G
(TTN)
|
ENSP00000340554.6:p.Val24475Gly
|
|
ENST00000342992.10:c.92339T>G
(TTN)
|
ENSP00000343764.6:p.Val30780Gly
|
|
ENST00000359218.9:c.73223T>G
(TTN)
|
ENSP00000352154.5:p.Val24408Gly
|
|
ENST00000460472.6:c.72848T>G
(TTN)
|
ENSP00000434586.1:p.Val24283Gly
|
|
ENST00000589042.5:c.100043T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Val33348Gly
|
|
ENST00000591111.5:c.95120T>G
(TTN)
|
ENSP00000465570.1:p.Val31707Gly
|
|
ENST00000615779.4:c.95120T>G
(TTN)
|
ENSP00000483597.1:p.Val31707Gly
|
|
NM_001256850.1:c.95120T>G
(TTN)
|
NP_001243779.1:p.Val31707Gly
|
|
NM_001267550.2:c.100043T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Val33348Gly
|
|
NM_003319.4:c.72848T>G
(TTN)
|
NP_003310.4:p.Val24283Gly
|
|
NM_133378.4:c.92339T>G
(TTN)
|
NP_596869.4:p.Val30780Gly
|
|
NM_133432.3:c.73223T>G
(TTN)
|
NP_597676.3:p.Val24408Gly
|
|
NM_133437.4:c.73424T>G
(TTN)
|
NP_597681.4:p.Val24475Gly
|
|
NR_038271.1:n.446+13430A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.317-295A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.99140T>G
(TTN)
|
XP_011510031.1:p.Val33047Gly
|
|
XM_011511730.1:c.73034T>G
(TTN)
|
XP_011510032.1:p.Val24345Gly
|
|
XM_011511731.1:c.72893T>G
(TTN)
|
XP_011510033.1:p.Val24298Gly
|
|
XM_017004819.1:c.98936T>G
(TTN)
|
XP_016860308.1:p.Val32979Gly
|
|
XM_017004820.1:c.94334T>G
(TTN)
|
XP_016860309.1:p.Val31445Gly
|
|
XM_017004821.1:c.94331T>G
(TTN)
|
XP_016860310.1:p.Val31444Gly
|
|
XM_017004822.1:c.91373T>G
(TTN)
|
XP_016860311.1:p.Val30458Gly
|
|
XM_017004823.1:c.72989T>G
(TTN)
|
XP_016860312.1:p.Val24330Gly
|
|
XM_024453094.1:c.94484T>G
(TTN)
|
XP_024308862.1:p.Val31495Gly
|
|
XM_024453095.1:c.94481T>G
(TTN)
|
XP_024308863.1:p.Val31494Gly
|
|
XM_024453096.1:c.93914T>G
(TTN)
|
XP_024308864.1:p.Val31305Gly
|
|
XM_024453097.1:c.91256T>G
(TTN)
|
XP_024308865.1:p.Val30419Gly
|
|
XM_024453098.1:c.91175T>G
(TTN)
|
XP_024308866.1:p.Val30392Gly
|
|
XM_024453099.1:c.72938T>G
(TTN)
|
XP_024308867.1:p.Val24313Gly
|
|
XM_024453100.1:c.62792T>G
(TTN)
|
XP_024308868.1:p.Val20931Gly
|
|