ENST00000342992.11:c.59919A>G
(TTN)
|
ENSP00000343764.6:p.Ala19973=
|
|
ENST00000342175.11:c.41004A>G
(TTN)
|
ENSP00000340554.6:p.Ala13668=
|
|
ENST00000359218.10:c.40803A>G
(TTN)
|
ENSP00000352154.5:p.Ala13601=
|
|
ENST00000342175.10:c.41004A>G
(TTN)
|
ENSP00000340554.6:p.Ala13668=
|
|
ENST00000342992.10:c.59919A>G
(TTN)
|
ENSP00000343764.6:p.Ala19973=
|
|
ENST00000359218.9:c.40803A>G
(TTN)
|
ENSP00000352154.5:p.Ala13601=
|
|
ENST00000460472.6:c.40428A>G
(TTN)
|
ENSP00000434586.1:p.Ala13476=
|
|
ENST00000589042.5:c.67623A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ala22541=
|
|
ENST00000591111.5:c.62700A>G
(TTN)
|
ENSP00000465570.1:p.Ala20900=
|
|
ENST00000615779.4:c.62700A>G
(TTN)
|
ENSP00000483597.1:p.Ala20900=
|
|
NM_001256850.1:c.62700A>G
(TTN)
|
NP_001243779.1:p.Ala20900=
|
|
NM_001267550.2:c.67623A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Ala22541=
|
|
NM_003319.4:c.40428A>G
(TTN)
|
NP_003310.4:p.Ala13476=
|
|
NM_133378.4:c.59919A>G
(TTN)
|
NP_596869.4:p.Ala19973=
|
|
NM_133432.3:c.40803A>G
(TTN)
|
NP_597676.3:p.Ala13601=
|
|
NM_133437.4:c.41004A>G
(TTN)
|
NP_597681.4:p.Ala13668=
|
|
NR_038271.1:n.596+8125T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-2998T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.66720A>G
(TTN)
|
XP_011510031.1:p.Ala22240=
|
|
XM_011511730.1:c.40614A>G
(TTN)
|
XP_011510032.1:p.Ala13538=
|
|
XM_011511731.1:c.40473A>G
(TTN)
|
XP_011510033.1:p.Ala13491=
|
|
XM_017004819.1:c.66516A>G
(TTN)
|
XP_016860308.1:p.Ala22172=
|
|
XM_017004820.1:c.61914A>G
(TTN)
|
XP_016860309.1:p.Ala20638=
|
|
XM_017004821.1:c.61911A>G
(TTN)
|
XP_016860310.1:p.Ala20637=
|
|
XM_017004822.1:c.58953A>G
(TTN)
|
XP_016860311.1:p.Ala19651=
|
|
XM_017004823.1:c.40569A>G
(TTN)
|
XP_016860312.1:p.Ala13523=
|
|
XM_024453094.1:c.62064A>G
(TTN)
|
XP_024308862.1:p.Ala20688=
|
|
XM_024453095.1:c.62061A>G
(TTN)
|
XP_024308863.1:p.Ala20687=
|
|
XM_024453096.1:c.61494A>G
(TTN)
|
XP_024308864.1:p.Ala20498=
|
|
XM_024453097.1:c.58836A>G
(TTN)
|
XP_024308865.1:p.Ala19612=
|
|
XM_024453098.1:c.58755A>G
(TTN)
|
XP_024308866.1:p.Ala19585=
|
|
XM_024453099.1:c.40518A>G
(TTN)
|
XP_024308867.1:p.Ala13506=
|
|
XM_024453100.1:c.30372A>G
(TTN)
|
XP_024308868.1:p.Ala10124=
|
|