ENST00000342992.11:c.96804A>T
(TTN)
|
ENSP00000343764.6:p.Leu32268=
|
|
ENST00000342175.11:c.77889A>T
(TTN)
|
ENSP00000340554.6:p.Leu25963=
|
|
ENST00000359218.10:c.77688A>T
(TTN)
|
ENSP00000352154.5:p.Leu25896=
|
|
ENST00000342175.10:c.77889A>T
(TTN)
|
ENSP00000340554.6:p.Leu25963=
|
|
ENST00000342992.10:c.96804A>T
(TTN)
|
ENSP00000343764.6:p.Leu32268=
|
|
ENST00000359218.9:c.77688A>T
(TTN)
|
ENSP00000352154.5:p.Leu25896=
|
|
ENST00000460472.6:c.77313A>T
(TTN)
|
ENSP00000434586.1:p.Leu25771=
|
|
ENST00000589042.5:c.104508A>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu34836=
|
|
ENST00000591111.5:c.99585A>T
(TTN)
|
ENSP00000465570.1:p.Leu33195=
|
|
ENST00000615779.4:c.99585A>T
(TTN)
|
ENSP00000483597.1:p.Leu33195=
|
|
NM_001256850.1:c.99585A>T
(TTN)
|
NP_001243779.1:p.Leu33195=
|
|
NM_001267550.2:c.104508A>T
(TTN)
MANE Select
|
NP_001254479.2:p.Leu34836=
|
|
NM_003319.4:c.77313A>T
(TTN)
|
NP_003310.4:p.Leu25771=
|
|
NM_133378.4:c.96804A>T
(TTN)
|
NP_596869.4:p.Leu32268=
|
|
NM_133432.3:c.77688A>T
(TTN)
|
NP_597676.3:p.Leu25896=
|
|
NM_133437.4:c.77889A>T
(TTN)
|
NP_597681.4:p.Leu25963=
|
|
NR_038271.1:n.446+8471T>A
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3625T>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.103605A>T
(TTN)
|
XP_011510031.1:p.Leu34535=
|
|
XM_011511730.1:c.77499A>T
(TTN)
|
XP_011510032.1:p.Leu25833=
|
|
XM_011511731.1:c.77358A>T
(TTN)
|
XP_011510033.1:p.Leu25786=
|
|
XM_017004819.1:c.103401A>T
(TTN)
|
XP_016860308.1:p.Leu34467=
|
|
XM_017004820.1:c.98799A>T
(TTN)
|
XP_016860309.1:p.Leu32933=
|
|
XM_017004821.1:c.98796A>T
(TTN)
|
XP_016860310.1:p.Leu32932=
|
|
XM_017004822.1:c.95838A>T
(TTN)
|
XP_016860311.1:p.Leu31946=
|
|
XM_017004823.1:c.77454A>T
(TTN)
|
XP_016860312.1:p.Leu25818=
|
|
XM_024453094.1:c.98949A>T
(TTN)
|
XP_024308862.1:p.Leu32983=
|
|
XM_024453095.1:c.98946A>T
(TTN)
|
XP_024308863.1:p.Leu32982=
|
|
XM_024453096.1:c.98379A>T
(TTN)
|
XP_024308864.1:p.Leu32793=
|
|
XM_024453097.1:c.95721A>T
(TTN)
|
XP_024308865.1:p.Leu31907=
|
|
XM_024453098.1:c.95640A>T
(TTN)
|
XP_024308866.1:p.Leu31880=
|
|
XM_024453099.1:c.77403A>T
(TTN)
|
XP_024308867.1:p.Leu25801=
|
|
XM_024453100.1:c.67257A>T
(TTN)
|
XP_024308868.1:p.Leu22419=
|
|