ENST00000342992.11:c.47359G>T
(TTN)
|
ENSP00000343764.6:p.Ala15787Ser
|
|
ENST00000342175.11:c.28444G>T
(TTN)
|
ENSP00000340554.6:p.Ala9482Ser
|
|
ENST00000359218.10:c.28243G>T
(TTN)
|
ENSP00000352154.5:p.Ala9415Ser
|
|
ENST00000342175.10:c.28444G>T
(TTN)
|
ENSP00000340554.6:p.Ala9482Ser
|
|
ENST00000342992.10:c.47359G>T
(TTN)
|
ENSP00000343764.6:p.Ala15787Ser
|
|
ENST00000359218.9:c.28243G>T
(TTN)
|
ENSP00000352154.5:p.Ala9415Ser
|
|
ENST00000460472.6:c.27868G>T
(TTN)
|
ENSP00000434586.1:p.Ala9290Ser
|
|
ENST00000589042.5:c.55063G>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ala18355Ser
|
|
ENST00000591111.5:c.50140G>T
(TTN)
|
ENSP00000465570.1:p.Ala16714Ser
|
|
ENST00000615779.4:c.50140G>T
(TTN)
|
ENSP00000483597.1:p.Ala16714Ser
|
|
NM_001256850.1:c.50140G>T
(TTN)
|
NP_001243779.1:p.Ala16714Ser
|
|
NM_001267550.2:c.55063G>T
(TTN)
MANE Select
|
NP_001254479.2:p.Ala18355Ser
|
|
NM_003319.4:c.27868G>T
(TTN)
|
NP_003310.4:p.Ala9290Ser
|
|
NM_133378.4:c.47359G>T
(TTN)
|
NP_596869.4:p.Ala15787Ser
|
|
NM_133432.3:c.28243G>T
(TTN)
|
NP_597676.3:p.Ala9415Ser
|
|
NM_133437.4:c.28444G>T
(TTN)
|
NP_597681.4:p.Ala9482Ser
|
|
NR_038271.1:n.682+4658C>A
(TTN-AS1)
|
|
|
NR_038272.1:n.3917+1672C>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.54160G>T
(TTN)
|
XP_011510031.1:p.Ala18054Ser
|
|
XM_011511730.1:c.28054G>T
(TTN)
|
XP_011510032.1:p.Ala9352Ser
|
|
XM_011511731.1:c.27913G>T
(TTN)
|
XP_011510033.1:p.Ala9305Ser
|
|
XM_017004819.1:c.53956G>T
(TTN)
|
XP_016860308.1:p.Ala17986Ser
|
|
XM_017004820.1:c.49354G>T
(TTN)
|
XP_016860309.1:p.Ala16452Ser
|
|
XM_017004821.1:c.49351G>T
(TTN)
|
XP_016860310.1:p.Ala16451Ser
|
|
XM_017004822.1:c.46393G>T
(TTN)
|
XP_016860311.1:p.Ala15465Ser
|
|
XM_017004823.1:c.28009G>T
(TTN)
|
XP_016860312.1:p.Ala9337Ser
|
|
XM_024453094.1:c.49504G>T
(TTN)
|
XP_024308862.1:p.Ala16502Ser
|
|
XM_024453095.1:c.49501G>T
(TTN)
|
XP_024308863.1:p.Ala16501Ser
|
|
XM_024453096.1:c.48934G>T
(TTN)
|
XP_024308864.1:p.Ala16312Ser
|
|
XM_024453097.1:c.46276G>T
(TTN)
|
XP_024308865.1:p.Ala15426Ser
|
|
XM_024453098.1:c.46195G>T
(TTN)
|
XP_024308866.1:p.Ala15399Ser
|
|
XM_024453099.1:c.27958G>T
(TTN)
|
XP_024308867.1:p.Ala9320Ser
|
|
XM_024453100.1:c.17812G>T
(TTN)
|
XP_024308868.1:p.Ala5938Ser
|
|