ENST00000342992.11:c.62866A>G
(TTN)
|
ENSP00000343764.6:p.Thr20956Ala
|
|
ENST00000342175.11:c.43951A>G
(TTN)
|
ENSP00000340554.6:p.Thr14651Ala
|
|
ENST00000359218.10:c.43750A>G
(TTN)
|
ENSP00000352154.5:p.Thr14584Ala
|
|
ENST00000342175.10:c.43951A>G
(TTN)
|
ENSP00000340554.6:p.Thr14651Ala
|
|
ENST00000342992.10:c.62866A>G
(TTN)
|
ENSP00000343764.6:p.Thr20956Ala
|
|
ENST00000359218.9:c.43750A>G
(TTN)
|
ENSP00000352154.5:p.Thr14584Ala
|
|
ENST00000460472.6:c.43375A>G
(TTN)
|
ENSP00000434586.1:p.Thr14459Ala
|
|
ENST00000589042.5:c.70570A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr23524Ala
|
|
ENST00000591111.5:c.65647A>G
(TTN)
|
ENSP00000465570.1:p.Thr21883Ala
|
|
ENST00000615779.4:c.65647A>G
(TTN)
|
ENSP00000483597.1:p.Thr21883Ala
|
|
NM_001256850.1:c.65647A>G
(TTN)
|
NP_001243779.1:p.Thr21883Ala
|
|
NM_001267550.2:c.70570A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Thr23524Ala
|
|
NM_003319.4:c.43375A>G
(TTN)
|
NP_003310.4:p.Thr14459Ala
|
|
NM_133378.4:c.62866A>G
(TTN)
|
NP_596869.4:p.Thr20956Ala
|
|
NM_133432.3:c.43750A>G
(TTN)
|
NP_597676.3:p.Thr14584Ala
|
|
NM_133437.4:c.43951A>G
(TTN)
|
NP_597681.4:p.Thr14651Ala
|
|
NR_038271.1:n.596+4113T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-7010T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.69667A>G
(TTN)
|
XP_011510031.1:p.Thr23223Ala
|
|
XM_011511730.1:c.43561A>G
(TTN)
|
XP_011510032.1:p.Thr14521Ala
|
|
XM_011511731.1:c.43420A>G
(TTN)
|
XP_011510033.1:p.Thr14474Ala
|
|
XM_017004819.1:c.69463A>G
(TTN)
|
XP_016860308.1:p.Thr23155Ala
|
|
XM_017004820.1:c.64861A>G
(TTN)
|
XP_016860309.1:p.Thr21621Ala
|
|
XM_017004821.1:c.64858A>G
(TTN)
|
XP_016860310.1:p.Thr21620Ala
|
|
XM_017004822.1:c.61900A>G
(TTN)
|
XP_016860311.1:p.Thr20634Ala
|
|
XM_017004823.1:c.43516A>G
(TTN)
|
XP_016860312.1:p.Thr14506Ala
|
|
XM_024453094.1:c.65011A>G
(TTN)
|
XP_024308862.1:p.Thr21671Ala
|
|
XM_024453095.1:c.65008A>G
(TTN)
|
XP_024308863.1:p.Thr21670Ala
|
|
XM_024453096.1:c.64441A>G
(TTN)
|
XP_024308864.1:p.Thr21481Ala
|
|
XM_024453097.1:c.61783A>G
(TTN)
|
XP_024308865.1:p.Thr20595Ala
|
|
XM_024453098.1:c.61702A>G
(TTN)
|
XP_024308866.1:p.Thr20568Ala
|
|
XM_024453099.1:c.43465A>G
(TTN)
|
XP_024308867.1:p.Thr14489Ala
|
|
XM_024453100.1:c.33319A>G
(TTN)
|
XP_024308868.1:p.Thr11107Ala
|
|