ENST00000342992.11:c.77905C>T
(TTN)
|
ENSP00000343764.6:p.Leu25969=
|
|
ENST00000342175.11:c.58990C>T
(TTN)
|
ENSP00000340554.6:p.Leu19664=
|
|
ENST00000359218.10:c.58789C>T
(TTN)
|
ENSP00000352154.5:p.Leu19597=
|
|
ENST00000342175.10:c.58990C>T
(TTN)
|
ENSP00000340554.6:p.Leu19664=
|
|
ENST00000342992.10:c.77905C>T
(TTN)
|
ENSP00000343764.6:p.Leu25969=
|
|
ENST00000359218.9:c.58789C>T
(TTN)
|
ENSP00000352154.5:p.Leu19597=
|
|
ENST00000460472.6:c.58414C>T
(TTN)
|
ENSP00000434586.1:p.Leu19472=
|
|
ENST00000589042.5:c.85609C>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu28537=
|
|
ENST00000591111.5:c.80686C>T
(TTN)
|
ENSP00000465570.1:p.Leu26896=
|
|
ENST00000615779.4:c.80686C>T
(TTN)
|
ENSP00000483597.1:p.Leu26896=
|
|
NM_001256850.1:c.80686C>T
(TTN)
|
NP_001243779.1:p.Leu26896=
|
|
NM_001267550.2:c.85609C>T
(TTN)
MANE Select
|
NP_001254479.2:p.Leu28537=
|
|
NM_003319.4:c.58414C>T
(TTN)
|
NP_003310.4:p.Leu19472=
|
|
NM_133378.4:c.77905C>T
(TTN)
|
NP_596869.4:p.Leu25969=
|
|
NM_133432.3:c.58789C>T
(TTN)
|
NP_597676.3:p.Leu19597=
|
|
NM_133437.4:c.58990C>T
(TTN)
|
NP_597681.4:p.Leu19664=
|
|
NR_038271.1:n.447-10777G>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+18162G>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.84706C>T
(TTN)
|
XP_011510031.1:p.Leu28236=
|
|
XM_011511730.1:c.58600C>T
(TTN)
|
XP_011510032.1:p.Leu19534=
|
|
XM_011511731.1:c.58459C>T
(TTN)
|
XP_011510033.1:p.Leu19487=
|
|
XM_017004819.1:c.84502C>T
(TTN)
|
XP_016860308.1:p.Leu28168=
|
|
XM_017004820.1:c.79900C>T
(TTN)
|
XP_016860309.1:p.Leu26634=
|
|
XM_017004821.1:c.79897C>T
(TTN)
|
XP_016860310.1:p.Leu26633=
|
|
XM_017004822.1:c.76939C>T
(TTN)
|
XP_016860311.1:p.Leu25647=
|
|
XM_017004823.1:c.58555C>T
(TTN)
|
XP_016860312.1:p.Leu19519=
|
|
XM_024453094.1:c.80050C>T
(TTN)
|
XP_024308862.1:p.Leu26684=
|
|
XM_024453095.1:c.80047C>T
(TTN)
|
XP_024308863.1:p.Leu26683=
|
|
XM_024453096.1:c.79480C>T
(TTN)
|
XP_024308864.1:p.Leu26494=
|
|
XM_024453097.1:c.76822C>T
(TTN)
|
XP_024308865.1:p.Leu25608=
|
|
XM_024453098.1:c.76741C>T
(TTN)
|
XP_024308866.1:p.Leu25581=
|
|
XM_024453099.1:c.58504C>T
(TTN)
|
XP_024308867.1:p.Leu19502=
|
|
XM_024453100.1:c.48358C>T
(TTN)
|
XP_024308868.1:p.Leu16120=
|
|