ENST00000342992.11:c.67971T>A
(TTN)
|
ENSP00000343764.6:p.Ala22657=
|
|
ENST00000342175.11:c.49056T>A
(TTN)
|
ENSP00000340554.6:p.Ala16352=
|
|
ENST00000359218.10:c.48855T>A
(TTN)
|
ENSP00000352154.5:p.Ala16285=
|
|
ENST00000342175.10:c.49056T>A
(TTN)
|
ENSP00000340554.6:p.Ala16352=
|
|
ENST00000342992.10:c.67971T>A
(TTN)
|
ENSP00000343764.6:p.Ala22657=
|
|
ENST00000359218.9:c.48855T>A
(TTN)
|
ENSP00000352154.5:p.Ala16285=
|
|
ENST00000460472.6:c.48480T>A
(TTN)
|
ENSP00000434586.1:p.Ala16160=
|
|
ENST00000589042.5:c.75675T>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ala25225=
|
|
ENST00000591111.5:c.70752T>A
(TTN)
|
ENSP00000465570.1:p.Ala23584=
|
|
ENST00000615779.4:c.70752T>A
(TTN)
|
ENSP00000483597.1:p.Ala23584=
|
|
NM_001256850.1:c.70752T>A
(TTN)
|
NP_001243779.1:p.Ala23584=
|
|
NM_001267550.2:c.75675T>A
(TTN)
MANE Select
|
NP_001254479.2:p.Ala25225=
|
|
NM_003319.4:c.48480T>A
(TTN)
|
NP_003310.4:p.Ala16160=
|
|
NM_133378.4:c.67971T>A
(TTN)
|
NP_596869.4:p.Ala22657=
|
|
NM_133432.3:c.48855T>A
(TTN)
|
NP_597676.3:p.Ala16285=
|
|
NM_133437.4:c.49056T>A
(TTN)
|
NP_597681.4:p.Ala16352=
|
|
NR_038271.1:n.447-843A>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-12115A>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.74772T>A
(TTN)
|
XP_011510031.1:p.Ala24924=
|
|
XM_011511730.1:c.48666T>A
(TTN)
|
XP_011510032.1:p.Ala16222=
|
|
XM_011511731.1:c.48525T>A
(TTN)
|
XP_011510033.1:p.Ala16175=
|
|
XM_017004819.1:c.74568T>A
(TTN)
|
XP_016860308.1:p.Ala24856=
|
|
XM_017004820.1:c.69966T>A
(TTN)
|
XP_016860309.1:p.Ala23322=
|
|
XM_017004821.1:c.69963T>A
(TTN)
|
XP_016860310.1:p.Ala23321=
|
|
XM_017004822.1:c.67005T>A
(TTN)
|
XP_016860311.1:p.Ala22335=
|
|
XM_017004823.1:c.48621T>A
(TTN)
|
XP_016860312.1:p.Ala16207=
|
|
XM_024453094.1:c.70116T>A
(TTN)
|
XP_024308862.1:p.Ala23372=
|
|
XM_024453095.1:c.70113T>A
(TTN)
|
XP_024308863.1:p.Ala23371=
|
|
XM_024453096.1:c.69546T>A
(TTN)
|
XP_024308864.1:p.Ala23182=
|
|
XM_024453097.1:c.66888T>A
(TTN)
|
XP_024308865.1:p.Ala22296=
|
|
XM_024453098.1:c.66807T>A
(TTN)
|
XP_024308866.1:p.Ala22269=
|
|
XM_024453099.1:c.48570T>A
(TTN)
|
XP_024308867.1:p.Ala16190=
|
|
XM_024453100.1:c.38424T>A
(TTN)
|
XP_024308868.1:p.Ala12808=
|
|