ENST00000342992.11:c.64557G>C
(TTN)
|
ENSP00000343764.6:p.Leu21519=
|
|
ENST00000342175.11:c.45642G>C
(TTN)
|
ENSP00000340554.6:p.Leu15214=
|
|
ENST00000359218.10:c.45441G>C
(TTN)
|
ENSP00000352154.5:p.Leu15147=
|
|
ENST00000342175.10:c.45642G>C
(TTN)
|
ENSP00000340554.6:p.Leu15214=
|
|
ENST00000342992.10:c.64557G>C
(TTN)
|
ENSP00000343764.6:p.Leu21519=
|
|
ENST00000359218.9:c.45441G>C
(TTN)
|
ENSP00000352154.5:p.Leu15147=
|
|
ENST00000460472.6:c.45066G>C
(TTN)
|
ENSP00000434586.1:p.Leu15022=
|
|
ENST00000589042.5:c.72261G>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu24087=
|
|
ENST00000591111.5:c.67338G>C
(TTN)
|
ENSP00000465570.1:p.Leu22446=
|
|
ENST00000615779.4:c.67338G>C
(TTN)
|
ENSP00000483597.1:p.Leu22446=
|
|
NM_001256850.1:c.67338G>C
(TTN)
|
NP_001243779.1:p.Leu22446=
|
|
NM_001267550.2:c.72261G>C
(TTN)
MANE Select
|
NP_001254479.2:p.Leu24087=
|
|
NM_003319.4:c.45066G>C
(TTN)
|
NP_003310.4:p.Leu15022=
|
|
NM_133378.4:c.64557G>C
(TTN)
|
NP_596869.4:p.Leu21519=
|
|
NM_133432.3:c.45441G>C
(TTN)
|
NP_597676.3:p.Leu15147=
|
|
NM_133437.4:c.45642G>C
(TTN)
|
NP_597681.4:p.Leu15214=
|
|
NR_038271.1:n.596+2422C>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-8701C>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.71358G>C
(TTN)
|
XP_011510031.1:p.Leu23786=
|
|
XM_011511730.1:c.45252G>C
(TTN)
|
XP_011510032.1:p.Leu15084=
|
|
XM_011511731.1:c.45111G>C
(TTN)
|
XP_011510033.1:p.Leu15037=
|
|
XM_017004819.1:c.71154G>C
(TTN)
|
XP_016860308.1:p.Leu23718=
|
|
XM_017004820.1:c.66552G>C
(TTN)
|
XP_016860309.1:p.Leu22184=
|
|
XM_017004821.1:c.66549G>C
(TTN)
|
XP_016860310.1:p.Leu22183=
|
|
XM_017004822.1:c.63591G>C
(TTN)
|
XP_016860311.1:p.Leu21197=
|
|
XM_017004823.1:c.45207G>C
(TTN)
|
XP_016860312.1:p.Leu15069=
|
|
XM_024453094.1:c.66702G>C
(TTN)
|
XP_024308862.1:p.Leu22234=
|
|
XM_024453095.1:c.66699G>C
(TTN)
|
XP_024308863.1:p.Leu22233=
|
|
XM_024453096.1:c.66132G>C
(TTN)
|
XP_024308864.1:p.Leu22044=
|
|
XM_024453097.1:c.63474G>C
(TTN)
|
XP_024308865.1:p.Leu21158=
|
|
XM_024453098.1:c.63393G>C
(TTN)
|
XP_024308866.1:p.Leu21131=
|
|
XM_024453099.1:c.45156G>C
(TTN)
|
XP_024308867.1:p.Leu15052=
|
|
XM_024453100.1:c.35010G>C
(TTN)
|
XP_024308868.1:p.Leu11670=
|
|