ENST00000342992.11:c.96653A>G
(TTN)
|
ENSP00000343764.6:p.Tyr32218Cys
|
|
ENST00000342175.11:c.77738A>G
(TTN)
|
ENSP00000340554.6:p.Tyr25913Cys
|
|
ENST00000359218.10:c.77537A>G
(TTN)
|
ENSP00000352154.5:p.Tyr25846Cys
|
|
ENST00000342175.10:c.77738A>G
(TTN)
|
ENSP00000340554.6:p.Tyr25913Cys
|
|
ENST00000342992.10:c.96653A>G
(TTN)
|
ENSP00000343764.6:p.Tyr32218Cys
|
|
ENST00000359218.9:c.77537A>G
(TTN)
|
ENSP00000352154.5:p.Tyr25846Cys
|
|
ENST00000460472.6:c.77162A>G
(TTN)
|
ENSP00000434586.1:p.Tyr25721Cys
|
|
ENST00000589042.5:c.104357A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Tyr34786Cys
|
|
ENST00000591111.5:c.99434A>G
(TTN)
|
ENSP00000465570.1:p.Tyr33145Cys
|
|
ENST00000615779.4:c.99434A>G
(TTN)
|
ENSP00000483597.1:p.Tyr33145Cys
|
|
NM_001256850.1:c.99434A>G
(TTN)
|
NP_001243779.1:p.Tyr33145Cys
|
|
NM_001267550.2:c.104357A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Tyr34786Cys
|
|
NM_003319.4:c.77162A>G
(TTN)
|
NP_003310.4:p.Tyr25721Cys
|
|
NM_133378.4:c.96653A>G
(TTN)
|
NP_596869.4:p.Tyr32218Cys
|
|
NM_133432.3:c.77537A>G
(TTN)
|
NP_597676.3:p.Tyr25846Cys
|
|
NM_133437.4:c.77738A>G
(TTN)
|
NP_597681.4:p.Tyr25913Cys
|
|
NR_038271.1:n.446+8622T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3474T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.103454A>G
(TTN)
|
XP_011510031.1:p.Tyr34485Cys
|
|
XM_011511730.1:c.77348A>G
(TTN)
|
XP_011510032.1:p.Tyr25783Cys
|
|
XM_011511731.1:c.77207A>G
(TTN)
|
XP_011510033.1:p.Tyr25736Cys
|
|
XM_017004819.1:c.103250A>G
(TTN)
|
XP_016860308.1:p.Tyr34417Cys
|
|
XM_017004820.1:c.98648A>G
(TTN)
|
XP_016860309.1:p.Tyr32883Cys
|
|
XM_017004821.1:c.98645A>G
(TTN)
|
XP_016860310.1:p.Tyr32882Cys
|
|
XM_017004822.1:c.95687A>G
(TTN)
|
XP_016860311.1:p.Tyr31896Cys
|
|
XM_017004823.1:c.77303A>G
(TTN)
|
XP_016860312.1:p.Tyr25768Cys
|
|
XM_024453094.1:c.98798A>G
(TTN)
|
XP_024308862.1:p.Tyr32933Cys
|
|
XM_024453095.1:c.98795A>G
(TTN)
|
XP_024308863.1:p.Tyr32932Cys
|
|
XM_024453096.1:c.98228A>G
(TTN)
|
XP_024308864.1:p.Tyr32743Cys
|
|
XM_024453097.1:c.95570A>G
(TTN)
|
XP_024308865.1:p.Tyr31857Cys
|
|
XM_024453098.1:c.95489A>G
(TTN)
|
XP_024308866.1:p.Tyr31830Cys
|
|
XM_024453099.1:c.77252A>G
(TTN)
|
XP_024308867.1:p.Tyr25751Cys
|
|
XM_024453100.1:c.67106A>G
(TTN)
|
XP_024308868.1:p.Tyr22369Cys
|
|