ENST00000342992.11:c.78685A>G
(TTN)
|
ENSP00000343764.6:p.Thr26229Ala
|
|
ENST00000342175.11:c.59770A>G
(TTN)
|
ENSP00000340554.6:p.Thr19924Ala
|
|
ENST00000359218.10:c.59569A>G
(TTN)
|
ENSP00000352154.5:p.Thr19857Ala
|
|
ENST00000342175.10:c.59770A>G
(TTN)
|
ENSP00000340554.6:p.Thr19924Ala
|
|
ENST00000342992.10:c.78685A>G
(TTN)
|
ENSP00000343764.6:p.Thr26229Ala
|
|
ENST00000359218.9:c.59569A>G
(TTN)
|
ENSP00000352154.5:p.Thr19857Ala
|
|
ENST00000460472.6:c.59194A>G
(TTN)
|
ENSP00000434586.1:p.Thr19732Ala
|
|
ENST00000589042.5:c.86389A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr28797Ala
|
|
ENST00000591111.5:c.81466A>G
(TTN)
|
ENSP00000465570.1:p.Thr27156Ala
|
|
ENST00000615779.4:c.81466A>G
(TTN)
|
ENSP00000483597.1:p.Thr27156Ala
|
|
NM_001256850.1:c.81466A>G
(TTN)
|
NP_001243779.1:p.Thr27156Ala
|
|
NM_001267550.2:c.86389A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Thr28797Ala
|
|
NM_003319.4:c.59194A>G
(TTN)
|
NP_003310.4:p.Thr19732Ala
|
|
NM_133378.4:c.78685A>G
(TTN)
|
NP_596869.4:p.Thr26229Ala
|
|
NM_133432.3:c.59569A>G
(TTN)
|
NP_597676.3:p.Thr19857Ala
|
|
NM_133437.4:c.59770A>G
(TTN)
|
NP_597681.4:p.Thr19924Ala
|
|
NR_038271.1:n.447-11557T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+17382T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.85486A>G
(TTN)
|
XP_011510031.1:p.Thr28496Ala
|
|
XM_011511730.1:c.59380A>G
(TTN)
|
XP_011510032.1:p.Thr19794Ala
|
|
XM_011511731.1:c.59239A>G
(TTN)
|
XP_011510033.1:p.Thr19747Ala
|
|
XM_017004819.1:c.85282A>G
(TTN)
|
XP_016860308.1:p.Thr28428Ala
|
|
XM_017004820.1:c.80680A>G
(TTN)
|
XP_016860309.1:p.Thr26894Ala
|
|
XM_017004821.1:c.80677A>G
(TTN)
|
XP_016860310.1:p.Thr26893Ala
|
|
XM_017004822.1:c.77719A>G
(TTN)
|
XP_016860311.1:p.Thr25907Ala
|
|
XM_017004823.1:c.59335A>G
(TTN)
|
XP_016860312.1:p.Thr19779Ala
|
|
XM_024453094.1:c.80830A>G
(TTN)
|
XP_024308862.1:p.Thr26944Ala
|
|
XM_024453095.1:c.80827A>G
(TTN)
|
XP_024308863.1:p.Thr26943Ala
|
|
XM_024453096.1:c.80260A>G
(TTN)
|
XP_024308864.1:p.Thr26754Ala
|
|
XM_024453097.1:c.77602A>G
(TTN)
|
XP_024308865.1:p.Thr25868Ala
|
|
XM_024453098.1:c.77521A>G
(TTN)
|
XP_024308866.1:p.Thr25841Ala
|
|
XM_024453099.1:c.59284A>G
(TTN)
|
XP_024308867.1:p.Thr19762Ala
|
|
XM_024453100.1:c.49138A>G
(TTN)
|
XP_024308868.1:p.Thr16380Ala
|
|