ENST00000342992.11:c.98749T>G
(TTN)
|
ENSP00000343764.6:p.Ser32917Ala
|
|
ENST00000342175.11:c.79834T>G
(TTN)
|
ENSP00000340554.6:p.Ser26612Ala
|
|
ENST00000359218.10:c.79633T>G
(TTN)
|
ENSP00000352154.5:p.Ser26545Ala
|
|
ENST00000342175.10:c.79834T>G
(TTN)
|
ENSP00000340554.6:p.Ser26612Ala
|
|
ENST00000342992.10:c.98749T>G
(TTN)
|
ENSP00000343764.6:p.Ser32917Ala
|
|
ENST00000359218.9:c.79633T>G
(TTN)
|
ENSP00000352154.5:p.Ser26545Ala
|
|
ENST00000460472.6:c.79258T>G
(TTN)
|
ENSP00000434586.1:p.Ser26420Ala
|
|
ENST00000589042.5:c.106453T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ser35485Ala
|
|
ENST00000591111.5:c.101530T>G
(TTN)
|
ENSP00000465570.1:p.Ser33844Ala
|
|
ENST00000615779.4:c.101530T>G
(TTN)
|
ENSP00000483597.1:p.Ser33844Ala
|
|
NM_001256850.1:c.101530T>G
(TTN)
|
NP_001243779.1:p.Ser33844Ala
|
|
NM_001267550.2:c.106453T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Ser35485Ala
|
|
NM_003319.4:c.79258T>G
(TTN)
|
NP_003310.4:p.Ser26420Ala
|
|
NM_133378.4:c.98749T>G
(TTN)
|
NP_596869.4:p.Ser32917Ala
|
|
NM_133432.3:c.79633T>G
(TTN)
|
NP_597676.3:p.Ser26545Ala
|
|
NM_133437.4:c.79834T>G
(TTN)
|
NP_597681.4:p.Ser26612Ala
|
|
NR_038271.1:n.446+6402A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5694A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.105550T>G
(TTN)
|
XP_011510031.1:p.Ser35184Ala
|
|
XM_011511730.1:c.79444T>G
(TTN)
|
XP_011510032.1:p.Ser26482Ala
|
|
XM_011511731.1:c.79303T>G
(TTN)
|
XP_011510033.1:p.Ser26435Ala
|
|
XM_017004819.1:c.105346T>G
(TTN)
|
XP_016860308.1:p.Ser35116Ala
|
|
XM_017004820.1:c.100744T>G
(TTN)
|
XP_016860309.1:p.Ser33582Ala
|
|
XM_017004821.1:c.100741T>G
(TTN)
|
XP_016860310.1:p.Ser33581Ala
|
|
XM_017004822.1:c.97783T>G
(TTN)
|
XP_016860311.1:p.Ser32595Ala
|
|
XM_017004823.1:c.79399T>G
(TTN)
|
XP_016860312.1:p.Ser26467Ala
|
|
XM_024453094.1:c.100894T>G
(TTN)
|
XP_024308862.1:p.Ser33632Ala
|
|
XM_024453095.1:c.100891T>G
(TTN)
|
XP_024308863.1:p.Ser33631Ala
|
|
XM_024453096.1:c.100324T>G
(TTN)
|
XP_024308864.1:p.Ser33442Ala
|
|
XM_024453097.1:c.97666T>G
(TTN)
|
XP_024308865.1:p.Ser32556Ala
|
|
XM_024453098.1:c.97585T>G
(TTN)
|
XP_024308866.1:p.Ser32529Ala
|
|
XM_024453099.1:c.79348T>G
(TTN)
|
XP_024308867.1:p.Ser26450Ala
|
|
XM_024453100.1:c.69202T>G
(TTN)
|
XP_024308868.1:p.Ser23068Ala
|
|