ENST00000342992.11:c.98700C>T
(TTN)
|
ENSP00000343764.6:p.Leu32900=
|
|
ENST00000342175.11:c.79785C>T
(TTN)
|
ENSP00000340554.6:p.Leu26595=
|
|
ENST00000359218.10:c.79584C>T
(TTN)
|
ENSP00000352154.5:p.Leu26528=
|
|
ENST00000342175.10:c.79785C>T
(TTN)
|
ENSP00000340554.6:p.Leu26595=
|
|
ENST00000342992.10:c.98700C>T
(TTN)
|
ENSP00000343764.6:p.Leu32900=
|
|
ENST00000359218.9:c.79584C>T
(TTN)
|
ENSP00000352154.5:p.Leu26528=
|
|
ENST00000460472.6:c.79209C>T
(TTN)
|
ENSP00000434586.1:p.Leu26403=
|
|
ENST00000589042.5:c.106404C>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu35468=
|
|
ENST00000591111.5:c.101481C>T
(TTN)
|
ENSP00000465570.1:p.Leu33827=
|
|
ENST00000615779.4:c.101481C>T
(TTN)
|
ENSP00000483597.1:p.Leu33827=
|
|
NM_001256850.1:c.101481C>T
(TTN)
|
NP_001243779.1:p.Leu33827=
|
|
NM_001267550.2:c.106404C>T
(TTN)
MANE Select
|
NP_001254479.2:p.Leu35468=
|
|
NM_003319.4:c.79209C>T
(TTN)
|
NP_003310.4:p.Leu26403=
|
|
NM_133378.4:c.98700C>T
(TTN)
|
NP_596869.4:p.Leu32900=
|
|
NM_133432.3:c.79584C>T
(TTN)
|
NP_597676.3:p.Leu26528=
|
|
NM_133437.4:c.79785C>T
(TTN)
|
NP_597681.4:p.Leu26595=
|
|
NR_038271.1:n.446+6451G>A
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5645G>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.105501C>T
(TTN)
|
XP_011510031.1:p.Leu35167=
|
|
XM_011511730.1:c.79395C>T
(TTN)
|
XP_011510032.1:p.Leu26465=
|
|
XM_011511731.1:c.79254C>T
(TTN)
|
XP_011510033.1:p.Leu26418=
|
|
XM_017004819.1:c.105297C>T
(TTN)
|
XP_016860308.1:p.Leu35099=
|
|
XM_017004820.1:c.100695C>T
(TTN)
|
XP_016860309.1:p.Leu33565=
|
|
XM_017004821.1:c.100692C>T
(TTN)
|
XP_016860310.1:p.Leu33564=
|
|
XM_017004822.1:c.97734C>T
(TTN)
|
XP_016860311.1:p.Leu32578=
|
|
XM_017004823.1:c.79350C>T
(TTN)
|
XP_016860312.1:p.Leu26450=
|
|
XM_024453094.1:c.100845C>T
(TTN)
|
XP_024308862.1:p.Leu33615=
|
|
XM_024453095.1:c.100842C>T
(TTN)
|
XP_024308863.1:p.Leu33614=
|
|
XM_024453096.1:c.100275C>T
(TTN)
|
XP_024308864.1:p.Leu33425=
|
|
XM_024453097.1:c.97617C>T
(TTN)
|
XP_024308865.1:p.Leu32539=
|
|
XM_024453098.1:c.97536C>T
(TTN)
|
XP_024308866.1:p.Leu32512=
|
|
XM_024453099.1:c.79299C>T
(TTN)
|
XP_024308867.1:p.Leu26433=
|
|
XM_024453100.1:c.69153C>T
(TTN)
|
XP_024308868.1:p.Leu23051=
|
|