ENST00000342992.11:c.67884T>G
(TTN)
|
ENSP00000343764.6:p.Thr22628=
|
|
ENST00000342175.11:c.48969T>G
(TTN)
|
ENSP00000340554.6:p.Thr16323=
|
|
ENST00000359218.10:c.48768T>G
(TTN)
|
ENSP00000352154.5:p.Thr16256=
|
|
ENST00000342175.10:c.48969T>G
(TTN)
|
ENSP00000340554.6:p.Thr16323=
|
|
ENST00000342992.10:c.67884T>G
(TTN)
|
ENSP00000343764.6:p.Thr22628=
|
|
ENST00000359218.9:c.48768T>G
(TTN)
|
ENSP00000352154.5:p.Thr16256=
|
|
ENST00000460472.6:c.48393T>G
(TTN)
|
ENSP00000434586.1:p.Thr16131=
|
|
ENST00000589042.5:c.75588T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr25196=
|
|
ENST00000591111.5:c.70665T>G
(TTN)
|
ENSP00000465570.1:p.Thr23555=
|
|
ENST00000615779.4:c.70665T>G
(TTN)
|
ENSP00000483597.1:p.Thr23555=
|
|
NM_001256850.1:c.70665T>G
(TTN)
|
NP_001243779.1:p.Thr23555=
|
|
NM_001267550.2:c.75588T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Thr25196=
|
|
NM_003319.4:c.48393T>G
(TTN)
|
NP_003310.4:p.Thr16131=
|
|
NM_133378.4:c.67884T>G
(TTN)
|
NP_596869.4:p.Thr22628=
|
|
NM_133432.3:c.48768T>G
(TTN)
|
NP_597676.3:p.Thr16256=
|
|
NM_133437.4:c.48969T>G
(TTN)
|
NP_597681.4:p.Thr16323=
|
|
NR_038271.1:n.447-756A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-12028A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.74685T>G
(TTN)
|
XP_011510031.1:p.Thr24895=
|
|
XM_011511730.1:c.48579T>G
(TTN)
|
XP_011510032.1:p.Thr16193=
|
|
XM_011511731.1:c.48438T>G
(TTN)
|
XP_011510033.1:p.Thr16146=
|
|
XM_017004819.1:c.74481T>G
(TTN)
|
XP_016860308.1:p.Thr24827=
|
|
XM_017004820.1:c.69879T>G
(TTN)
|
XP_016860309.1:p.Thr23293=
|
|
XM_017004821.1:c.69876T>G
(TTN)
|
XP_016860310.1:p.Thr23292=
|
|
XM_017004822.1:c.66918T>G
(TTN)
|
XP_016860311.1:p.Thr22306=
|
|
XM_017004823.1:c.48534T>G
(TTN)
|
XP_016860312.1:p.Thr16178=
|
|
XM_024453094.1:c.70029T>G
(TTN)
|
XP_024308862.1:p.Thr23343=
|
|
XM_024453095.1:c.70026T>G
(TTN)
|
XP_024308863.1:p.Thr23342=
|
|
XM_024453096.1:c.69459T>G
(TTN)
|
XP_024308864.1:p.Thr23153=
|
|
XM_024453097.1:c.66801T>G
(TTN)
|
XP_024308865.1:p.Thr22267=
|
|
XM_024453098.1:c.66720T>G
(TTN)
|
XP_024308866.1:p.Thr22240=
|
|
XM_024453099.1:c.48483T>G
(TTN)
|
XP_024308867.1:p.Thr16161=
|
|
XM_024453100.1:c.38337T>G
(TTN)
|
XP_024308868.1:p.Thr12779=
|
|