ENST00000342992.11:c.98404A>G
(TTN)
|
ENSP00000343764.6:p.Thr32802Ala
|
|
ENST00000342175.11:c.79489A>G
(TTN)
|
ENSP00000340554.6:p.Thr26497Ala
|
|
ENST00000359218.10:c.79288A>G
(TTN)
|
ENSP00000352154.5:p.Thr26430Ala
|
|
ENST00000342175.10:c.79489A>G
(TTN)
|
ENSP00000340554.6:p.Thr26497Ala
|
|
ENST00000342992.10:c.98404A>G
(TTN)
|
ENSP00000343764.6:p.Thr32802Ala
|
|
ENST00000359218.9:c.79288A>G
(TTN)
|
ENSP00000352154.5:p.Thr26430Ala
|
|
ENST00000460472.6:c.78913A>G
(TTN)
|
ENSP00000434586.1:p.Thr26305Ala
|
|
ENST00000589042.5:c.106108A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr35370Ala
|
|
ENST00000591111.5:c.101185A>G
(TTN)
|
ENSP00000465570.1:p.Thr33729Ala
|
|
ENST00000615779.4:c.101185A>G
(TTN)
|
ENSP00000483597.1:p.Thr33729Ala
|
|
NM_001256850.1:c.101185A>G
(TTN)
|
NP_001243779.1:p.Thr33729Ala
|
|
NM_001267550.2:c.106108A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Thr35370Ala
|
|
NM_003319.4:c.78913A>G
(TTN)
|
NP_003310.4:p.Thr26305Ala
|
|
NM_133378.4:c.98404A>G
(TTN)
|
NP_596869.4:p.Thr32802Ala
|
|
NM_133432.3:c.79288A>G
(TTN)
|
NP_597676.3:p.Thr26430Ala
|
|
NM_133437.4:c.79489A>G
(TTN)
|
NP_597681.4:p.Thr26497Ala
|
|
NR_038271.1:n.446+6871T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5225T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.105205A>G
(TTN)
|
XP_011510031.1:p.Thr35069Ala
|
|
XM_011511730.1:c.79099A>G
(TTN)
|
XP_011510032.1:p.Thr26367Ala
|
|
XM_011511731.1:c.78958A>G
(TTN)
|
XP_011510033.1:p.Thr26320Ala
|
|
XM_017004819.1:c.105001A>G
(TTN)
|
XP_016860308.1:p.Thr35001Ala
|
|
XM_017004820.1:c.100399A>G
(TTN)
|
XP_016860309.1:p.Thr33467Ala
|
|
XM_017004821.1:c.100396A>G
(TTN)
|
XP_016860310.1:p.Thr33466Ala
|
|
XM_017004822.1:c.97438A>G
(TTN)
|
XP_016860311.1:p.Thr32480Ala
|
|
XM_017004823.1:c.79054A>G
(TTN)
|
XP_016860312.1:p.Thr26352Ala
|
|
XM_024453094.1:c.100549A>G
(TTN)
|
XP_024308862.1:p.Thr33517Ala
|
|
XM_024453095.1:c.100546A>G
(TTN)
|
XP_024308863.1:p.Thr33516Ala
|
|
XM_024453096.1:c.99979A>G
(TTN)
|
XP_024308864.1:p.Thr33327Ala
|
|
XM_024453097.1:c.97321A>G
(TTN)
|
XP_024308865.1:p.Thr32441Ala
|
|
XM_024453098.1:c.97240A>G
(TTN)
|
XP_024308866.1:p.Thr32414Ala
|
|
XM_024453099.1:c.79003A>G
(TTN)
|
XP_024308867.1:p.Thr26335Ala
|
|
XM_024453100.1:c.68857A>G
(TTN)
|
XP_024308868.1:p.Thr22953Ala
|
|