ENST00000342992.11:c.96666T>G
(TTN)
|
ENSP00000343764.6:p.Leu32222=
|
|
ENST00000342175.11:c.77751T>G
(TTN)
|
ENSP00000340554.6:p.Leu25917=
|
|
ENST00000359218.10:c.77550T>G
(TTN)
|
ENSP00000352154.5:p.Leu25850=
|
|
ENST00000342175.10:c.77751T>G
(TTN)
|
ENSP00000340554.6:p.Leu25917=
|
|
ENST00000342992.10:c.96666T>G
(TTN)
|
ENSP00000343764.6:p.Leu32222=
|
|
ENST00000359218.9:c.77550T>G
(TTN)
|
ENSP00000352154.5:p.Leu25850=
|
|
ENST00000460472.6:c.77175T>G
(TTN)
|
ENSP00000434586.1:p.Leu25725=
|
|
ENST00000589042.5:c.104370T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu34790=
|
|
ENST00000591111.5:c.99447T>G
(TTN)
|
ENSP00000465570.1:p.Leu33149=
|
|
ENST00000615779.4:c.99447T>G
(TTN)
|
ENSP00000483597.1:p.Leu33149=
|
|
NM_001256850.1:c.99447T>G
(TTN)
|
NP_001243779.1:p.Leu33149=
|
|
NM_001267550.2:c.104370T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Leu34790=
|
|
NM_003319.4:c.77175T>G
(TTN)
|
NP_003310.4:p.Leu25725=
|
|
NM_133378.4:c.96666T>G
(TTN)
|
NP_596869.4:p.Leu32222=
|
|
NM_133432.3:c.77550T>G
(TTN)
|
NP_597676.3:p.Leu25850=
|
|
NM_133437.4:c.77751T>G
(TTN)
|
NP_597681.4:p.Leu25917=
|
|
NR_038271.1:n.446+8609A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3487A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.103467T>G
(TTN)
|
XP_011510031.1:p.Leu34489=
|
|
XM_011511730.1:c.77361T>G
(TTN)
|
XP_011510032.1:p.Leu25787=
|
|
XM_011511731.1:c.77220T>G
(TTN)
|
XP_011510033.1:p.Leu25740=
|
|
XM_017004819.1:c.103263T>G
(TTN)
|
XP_016860308.1:p.Leu34421=
|
|
XM_017004820.1:c.98661T>G
(TTN)
|
XP_016860309.1:p.Leu32887=
|
|
XM_017004821.1:c.98658T>G
(TTN)
|
XP_016860310.1:p.Leu32886=
|
|
XM_017004822.1:c.95700T>G
(TTN)
|
XP_016860311.1:p.Leu31900=
|
|
XM_017004823.1:c.77316T>G
(TTN)
|
XP_016860312.1:p.Leu25772=
|
|
XM_024453094.1:c.98811T>G
(TTN)
|
XP_024308862.1:p.Leu32937=
|
|
XM_024453095.1:c.98808T>G
(TTN)
|
XP_024308863.1:p.Leu32936=
|
|
XM_024453096.1:c.98241T>G
(TTN)
|
XP_024308864.1:p.Leu32747=
|
|
XM_024453097.1:c.95583T>G
(TTN)
|
XP_024308865.1:p.Leu31861=
|
|
XM_024453098.1:c.95502T>G
(TTN)
|
XP_024308866.1:p.Leu31834=
|
|
XM_024453099.1:c.77265T>G
(TTN)
|
XP_024308867.1:p.Leu25755=
|
|
XM_024453100.1:c.67119T>G
(TTN)
|
XP_024308868.1:p.Leu22373=
|
|