ENST00000342992.11:c.98389G>A
(TTN)
|
ENSP00000343764.6:p.Gly32797Ser
|
|
ENST00000342175.11:c.79474G>A
(TTN)
|
ENSP00000340554.6:p.Gly26492Ser
|
|
ENST00000359218.10:c.79273G>A
(TTN)
|
ENSP00000352154.5:p.Gly26425Ser
|
|
ENST00000342175.10:c.79474G>A
(TTN)
|
ENSP00000340554.6:p.Gly26492Ser
|
|
ENST00000342992.10:c.98389G>A
(TTN)
|
ENSP00000343764.6:p.Gly32797Ser
|
|
ENST00000359218.9:c.79273G>A
(TTN)
|
ENSP00000352154.5:p.Gly26425Ser
|
|
ENST00000460472.6:c.78898G>A
(TTN)
|
ENSP00000434586.1:p.Gly26300Ser
|
|
ENST00000589042.5:c.106093G>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gly35365Ser
|
|
ENST00000591111.5:c.101170G>A
(TTN)
|
ENSP00000465570.1:p.Gly33724Ser
|
|
ENST00000615779.4:c.101170G>A
(TTN)
|
ENSP00000483597.1:p.Gly33724Ser
|
|
NM_001256850.1:c.101170G>A
(TTN)
|
NP_001243779.1:p.Gly33724Ser
|
|
NM_001267550.2:c.106093G>A
(TTN)
MANE Select
|
NP_001254479.2:p.Gly35365Ser
|
|
NM_003319.4:c.78898G>A
(TTN)
|
NP_003310.4:p.Gly26300Ser
|
|
NM_133378.4:c.98389G>A
(TTN)
|
NP_596869.4:p.Gly32797Ser
|
|
NM_133432.3:c.79273G>A
(TTN)
|
NP_597676.3:p.Gly26425Ser
|
|
NM_133437.4:c.79474G>A
(TTN)
|
NP_597681.4:p.Gly26492Ser
|
|
NR_038271.1:n.446+6886C>T
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5210C>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.105190G>A
(TTN)
|
XP_011510031.1:p.Gly35064Ser
|
|
XM_011511730.1:c.79084G>A
(TTN)
|
XP_011510032.1:p.Gly26362Ser
|
|
XM_011511731.1:c.78943G>A
(TTN)
|
XP_011510033.1:p.Gly26315Ser
|
|
XM_017004819.1:c.104986G>A
(TTN)
|
XP_016860308.1:p.Gly34996Ser
|
|
XM_017004820.1:c.100384G>A
(TTN)
|
XP_016860309.1:p.Gly33462Ser
|
|
XM_017004821.1:c.100381G>A
(TTN)
|
XP_016860310.1:p.Gly33461Ser
|
|
XM_017004822.1:c.97423G>A
(TTN)
|
XP_016860311.1:p.Gly32475Ser
|
|
XM_017004823.1:c.79039G>A
(TTN)
|
XP_016860312.1:p.Gly26347Ser
|
|
XM_024453094.1:c.100534G>A
(TTN)
|
XP_024308862.1:p.Gly33512Ser
|
|
XM_024453095.1:c.100531G>A
(TTN)
|
XP_024308863.1:p.Gly33511Ser
|
|
XM_024453096.1:c.99964G>A
(TTN)
|
XP_024308864.1:p.Gly33322Ser
|
|
XM_024453097.1:c.97306G>A
(TTN)
|
XP_024308865.1:p.Gly32436Ser
|
|
XM_024453098.1:c.97225G>A
(TTN)
|
XP_024308866.1:p.Gly32409Ser
|
|
XM_024453099.1:c.78988G>A
(TTN)
|
XP_024308867.1:p.Gly26330Ser
|
|
XM_024453100.1:c.68842G>A
(TTN)
|
XP_024308868.1:p.Gly22948Ser
|
|