ENST00000342992.11:c.78793G>T
(TTN)
|
ENSP00000343764.6:p.Ala26265Ser
|
|
ENST00000342175.11:c.59878G>T
(TTN)
|
ENSP00000340554.6:p.Ala19960Ser
|
|
ENST00000359218.10:c.59677G>T
(TTN)
|
ENSP00000352154.5:p.Ala19893Ser
|
|
ENST00000342175.10:c.59878G>T
(TTN)
|
ENSP00000340554.6:p.Ala19960Ser
|
|
ENST00000342992.10:c.78793G>T
(TTN)
|
ENSP00000343764.6:p.Ala26265Ser
|
|
ENST00000359218.9:c.59677G>T
(TTN)
|
ENSP00000352154.5:p.Ala19893Ser
|
|
ENST00000460472.6:c.59302G>T
(TTN)
|
ENSP00000434586.1:p.Ala19768Ser
|
|
ENST00000589042.5:c.86497G>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ala28833Ser
|
|
ENST00000591111.5:c.81574G>T
(TTN)
|
ENSP00000465570.1:p.Ala27192Ser
|
|
ENST00000615779.4:c.81574G>T
(TTN)
|
ENSP00000483597.1:p.Ala27192Ser
|
|
NM_001256850.1:c.81574G>T
(TTN)
|
NP_001243779.1:p.Ala27192Ser
|
|
NM_001267550.2:c.86497G>T
(TTN)
MANE Select
|
NP_001254479.2:p.Ala28833Ser
|
|
NM_003319.4:c.59302G>T
(TTN)
|
NP_003310.4:p.Ala19768Ser
|
|
NM_133378.4:c.78793G>T
(TTN)
|
NP_596869.4:p.Ala26265Ser
|
|
NM_133432.3:c.59677G>T
(TTN)
|
NP_597676.3:p.Ala19893Ser
|
|
NM_133437.4:c.59878G>T
(TTN)
|
NP_597681.4:p.Ala19960Ser
|
|
NR_038271.1:n.447-11665C>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+17274C>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.85594G>T
(TTN)
|
XP_011510031.1:p.Ala28532Ser
|
|
XM_011511730.1:c.59488G>T
(TTN)
|
XP_011510032.1:p.Ala19830Ser
|
|
XM_011511731.1:c.59347G>T
(TTN)
|
XP_011510033.1:p.Ala19783Ser
|
|
XM_017004819.1:c.85390G>T
(TTN)
|
XP_016860308.1:p.Ala28464Ser
|
|
XM_017004820.1:c.80788G>T
(TTN)
|
XP_016860309.1:p.Ala26930Ser
|
|
XM_017004821.1:c.80785G>T
(TTN)
|
XP_016860310.1:p.Ala26929Ser
|
|
XM_017004822.1:c.77827G>T
(TTN)
|
XP_016860311.1:p.Ala25943Ser
|
|
XM_017004823.1:c.59443G>T
(TTN)
|
XP_016860312.1:p.Ala19815Ser
|
|
XM_024453094.1:c.80938G>T
(TTN)
|
XP_024308862.1:p.Ala26980Ser
|
|
XM_024453095.1:c.80935G>T
(TTN)
|
XP_024308863.1:p.Ala26979Ser
|
|
XM_024453096.1:c.80368G>T
(TTN)
|
XP_024308864.1:p.Ala26790Ser
|
|
XM_024453097.1:c.77710G>T
(TTN)
|
XP_024308865.1:p.Ala25904Ser
|
|
XM_024453098.1:c.77629G>T
(TTN)
|
XP_024308866.1:p.Ala25877Ser
|
|
XM_024453099.1:c.59392G>T
(TTN)
|
XP_024308867.1:p.Ala19798Ser
|
|
XM_024453100.1:c.49246G>T
(TTN)
|
XP_024308868.1:p.Ala16416Ser
|
|