ENST00000342992.11:c.98746A>G
(TTN)
|
ENSP00000343764.6:p.Thr32916Ala
|
|
ENST00000342175.11:c.79831A>G
(TTN)
|
ENSP00000340554.6:p.Thr26611Ala
|
|
ENST00000359218.10:c.79630A>G
(TTN)
|
ENSP00000352154.5:p.Thr26544Ala
|
|
ENST00000342175.10:c.79831A>G
(TTN)
|
ENSP00000340554.6:p.Thr26611Ala
|
|
ENST00000342992.10:c.98746A>G
(TTN)
|
ENSP00000343764.6:p.Thr32916Ala
|
|
ENST00000359218.9:c.79630A>G
(TTN)
|
ENSP00000352154.5:p.Thr26544Ala
|
|
ENST00000460472.6:c.79255A>G
(TTN)
|
ENSP00000434586.1:p.Thr26419Ala
|
|
ENST00000589042.5:c.106450A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr35484Ala
|
|
ENST00000591111.5:c.101527A>G
(TTN)
|
ENSP00000465570.1:p.Thr33843Ala
|
|
ENST00000615779.4:c.101527A>G
(TTN)
|
ENSP00000483597.1:p.Thr33843Ala
|
|
NM_001256850.1:c.101527A>G
(TTN)
|
NP_001243779.1:p.Thr33843Ala
|
|
NM_001267550.2:c.106450A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Thr35484Ala
|
|
NM_003319.4:c.79255A>G
(TTN)
|
NP_003310.4:p.Thr26419Ala
|
|
NM_133378.4:c.98746A>G
(TTN)
|
NP_596869.4:p.Thr32916Ala
|
|
NM_133432.3:c.79630A>G
(TTN)
|
NP_597676.3:p.Thr26544Ala
|
|
NM_133437.4:c.79831A>G
(TTN)
|
NP_597681.4:p.Thr26611Ala
|
|
NR_038271.1:n.446+6405T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5691T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.105547A>G
(TTN)
|
XP_011510031.1:p.Thr35183Ala
|
|
XM_011511730.1:c.79441A>G
(TTN)
|
XP_011510032.1:p.Thr26481Ala
|
|
XM_011511731.1:c.79300A>G
(TTN)
|
XP_011510033.1:p.Thr26434Ala
|
|
XM_017004819.1:c.105343A>G
(TTN)
|
XP_016860308.1:p.Thr35115Ala
|
|
XM_017004820.1:c.100741A>G
(TTN)
|
XP_016860309.1:p.Thr33581Ala
|
|
XM_017004821.1:c.100738A>G
(TTN)
|
XP_016860310.1:p.Thr33580Ala
|
|
XM_017004822.1:c.97780A>G
(TTN)
|
XP_016860311.1:p.Thr32594Ala
|
|
XM_017004823.1:c.79396A>G
(TTN)
|
XP_016860312.1:p.Thr26466Ala
|
|
XM_024453094.1:c.100891A>G
(TTN)
|
XP_024308862.1:p.Thr33631Ala
|
|
XM_024453095.1:c.100888A>G
(TTN)
|
XP_024308863.1:p.Thr33630Ala
|
|
XM_024453096.1:c.100321A>G
(TTN)
|
XP_024308864.1:p.Thr33441Ala
|
|
XM_024453097.1:c.97663A>G
(TTN)
|
XP_024308865.1:p.Thr32555Ala
|
|
XM_024453098.1:c.97582A>G
(TTN)
|
XP_024308866.1:p.Thr32528Ala
|
|
XM_024453099.1:c.79345A>G
(TTN)
|
XP_024308867.1:p.Thr26449Ala
|
|
XM_024453100.1:c.69199A>G
(TTN)
|
XP_024308868.1:p.Thr23067Ala
|
|