ENST00000342992.11:c.60809C>A
(TTN)
|
ENSP00000343764.6:p.Ala20270Glu
|
|
ENST00000342175.11:c.41894C>A
(TTN)
|
ENSP00000340554.6:p.Ala13965Glu
|
|
ENST00000359218.10:c.41693C>A
(TTN)
|
ENSP00000352154.5:p.Ala13898Glu
|
|
ENST00000342175.10:c.41894C>A
(TTN)
|
ENSP00000340554.6:p.Ala13965Glu
|
|
ENST00000342992.10:c.60809C>A
(TTN)
|
ENSP00000343764.6:p.Ala20270Glu
|
|
ENST00000359218.9:c.41693C>A
(TTN)
|
ENSP00000352154.5:p.Ala13898Glu
|
|
ENST00000460472.6:c.41318C>A
(TTN)
|
ENSP00000434586.1:p.Ala13773Glu
|
|
ENST00000589042.5:c.68513C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ala22838Glu
|
|
ENST00000591111.5:c.63590C>A
(TTN)
|
ENSP00000465570.1:p.Ala21197Glu
|
|
ENST00000615779.4:c.63590C>A
(TTN)
|
ENSP00000483597.1:p.Ala21197Glu
|
|
NM_001256850.1:c.63590C>A
(TTN)
|
NP_001243779.1:p.Ala21197Glu
|
|
NM_001267550.2:c.68513C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Ala22838Glu
|
|
NM_003319.4:c.41318C>A
(TTN)
|
NP_003310.4:p.Ala13773Glu
|
|
NM_133378.4:c.60809C>A
(TTN)
|
NP_596869.4:p.Ala20270Glu
|
|
NM_133432.3:c.41693C>A
(TTN)
|
NP_597676.3:p.Ala13898Glu
|
|
NM_133437.4:c.41894C>A
(TTN)
|
NP_597681.4:p.Ala13965Glu
|
|
NR_038271.1:n.596+6553G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-4570G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.67610C>A
(TTN)
|
XP_011510031.1:p.Ala22537Glu
|
|
XM_011511730.1:c.41504C>A
(TTN)
|
XP_011510032.1:p.Ala13835Glu
|
|
XM_011511731.1:c.41363C>A
(TTN)
|
XP_011510033.1:p.Ala13788Glu
|
|
XM_017004819.1:c.67406C>A
(TTN)
|
XP_016860308.1:p.Ala22469Glu
|
|
XM_017004820.1:c.62804C>A
(TTN)
|
XP_016860309.1:p.Ala20935Glu
|
|
XM_017004821.1:c.62801C>A
(TTN)
|
XP_016860310.1:p.Ala20934Glu
|
|
XM_017004822.1:c.59843C>A
(TTN)
|
XP_016860311.1:p.Ala19948Glu
|
|
XM_017004823.1:c.41459C>A
(TTN)
|
XP_016860312.1:p.Ala13820Glu
|
|
XM_024453094.1:c.62954C>A
(TTN)
|
XP_024308862.1:p.Ala20985Glu
|
|
XM_024453095.1:c.62951C>A
(TTN)
|
XP_024308863.1:p.Ala20984Glu
|
|
XM_024453096.1:c.62384C>A
(TTN)
|
XP_024308864.1:p.Ala20795Glu
|
|
XM_024453097.1:c.59726C>A
(TTN)
|
XP_024308865.1:p.Ala19909Glu
|
|
XM_024453098.1:c.59645C>A
(TTN)
|
XP_024308866.1:p.Ala19882Glu
|
|
XM_024453099.1:c.41408C>A
(TTN)
|
XP_024308867.1:p.Ala13803Glu
|
|
XM_024453100.1:c.31262C>A
(TTN)
|
XP_024308868.1:p.Ala10421Glu
|
|