ENST00000342992.11:c.85156A>G
(TTN)
|
ENSP00000343764.6:p.Thr28386Ala
|
|
ENST00000342175.11:c.66241A>G
(TTN)
|
ENSP00000340554.6:p.Thr22081Ala
|
|
ENST00000359218.10:c.66040A>G
(TTN)
|
ENSP00000352154.5:p.Thr22014Ala
|
|
ENST00000342175.10:c.66241A>G
(TTN)
|
ENSP00000340554.6:p.Thr22081Ala
|
|
ENST00000342992.10:c.85156A>G
(TTN)
|
ENSP00000343764.6:p.Thr28386Ala
|
|
ENST00000359218.9:c.66040A>G
(TTN)
|
ENSP00000352154.5:p.Thr22014Ala
|
|
ENST00000460472.6:c.65665A>G
(TTN)
|
ENSP00000434586.1:p.Thr21889Ala
|
|
ENST00000589042.5:c.92860A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr30954Ala
|
|
ENST00000591111.5:c.87937A>G
(TTN)
|
ENSP00000465570.1:p.Thr29313Ala
|
|
ENST00000615779.4:c.87937A>G
(TTN)
|
ENSP00000483597.1:p.Thr29313Ala
|
|
NM_001256850.1:c.87937A>G
(TTN)
|
NP_001243779.1:p.Thr29313Ala
|
|
NM_001267550.2:c.92860A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Thr30954Ala
|
|
NM_003319.4:c.65665A>G
(TTN)
|
NP_003310.4:p.Thr21889Ala
|
|
NM_133378.4:c.85156A>G
(TTN)
|
NP_596869.4:p.Thr28386Ala
|
|
NM_133432.3:c.66040A>G
(TTN)
|
NP_597676.3:p.Thr22014Ala
|
|
NM_133437.4:c.66241A>G
(TTN)
|
NP_597681.4:p.Thr22081Ala
|
|
NR_038271.1:n.447-22534T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+6405T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.91957A>G
(TTN)
|
XP_011510031.1:p.Thr30653Ala
|
|
XM_011511730.1:c.65851A>G
(TTN)
|
XP_011510032.1:p.Thr21951Ala
|
|
XM_011511731.1:c.65710A>G
(TTN)
|
XP_011510033.1:p.Thr21904Ala
|
|
XM_017004819.1:c.91753A>G
(TTN)
|
XP_016860308.1:p.Thr30585Ala
|
|
XM_017004820.1:c.87151A>G
(TTN)
|
XP_016860309.1:p.Thr29051Ala
|
|
XM_017004821.1:c.87148A>G
(TTN)
|
XP_016860310.1:p.Thr29050Ala
|
|
XM_017004822.1:c.84190A>G
(TTN)
|
XP_016860311.1:p.Thr28064Ala
|
|
XM_017004823.1:c.65806A>G
(TTN)
|
XP_016860312.1:p.Thr21936Ala
|
|
XM_024453094.1:c.87301A>G
(TTN)
|
XP_024308862.1:p.Thr29101Ala
|
|
XM_024453095.1:c.87298A>G
(TTN)
|
XP_024308863.1:p.Thr29100Ala
|
|
XM_024453096.1:c.86731A>G
(TTN)
|
XP_024308864.1:p.Thr28911Ala
|
|
XM_024453097.1:c.84073A>G
(TTN)
|
XP_024308865.1:p.Thr28025Ala
|
|
XM_024453098.1:c.83992A>G
(TTN)
|
XP_024308866.1:p.Thr27998Ala
|
|
XM_024453099.1:c.65755A>G
(TTN)
|
XP_024308867.1:p.Thr21919Ala
|
|
XM_024453100.1:c.55609A>G
(TTN)
|
XP_024308868.1:p.Thr18537Ala
|
|