ENST00000342992.11:c.86183T>C
(TTN)
|
ENSP00000343764.6:p.Val28728Ala
|
|
ENST00000342175.11:c.67268T>C
(TTN)
|
ENSP00000340554.6:p.Val22423Ala
|
|
ENST00000359218.10:c.67067T>C
(TTN)
|
ENSP00000352154.5:p.Val22356Ala
|
|
ENST00000342175.10:c.67268T>C
(TTN)
|
ENSP00000340554.6:p.Val22423Ala
|
|
ENST00000342992.10:c.86183T>C
(TTN)
|
ENSP00000343764.6:p.Val28728Ala
|
|
ENST00000359218.9:c.67067T>C
(TTN)
|
ENSP00000352154.5:p.Val22356Ala
|
|
ENST00000460472.6:c.66692T>C
(TTN)
|
ENSP00000434586.1:p.Val22231Ala
|
|
ENST00000589042.5:c.93887T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Val31296Ala
|
|
ENST00000591111.5:c.88964T>C
(TTN)
|
ENSP00000465570.1:p.Val29655Ala
|
|
ENST00000615779.4:c.88964T>C
(TTN)
|
ENSP00000483597.1:p.Val29655Ala
|
|
NM_001256850.1:c.88964T>C
(TTN)
|
NP_001243779.1:p.Val29655Ala
|
|
NM_001267550.2:c.93887T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Val31296Ala
|
|
NM_003319.4:c.66692T>C
(TTN)
|
NP_003310.4:p.Val22231Ala
|
|
NM_133378.4:c.86183T>C
(TTN)
|
NP_596869.4:p.Val28728Ala
|
|
NM_133432.3:c.67067T>C
(TTN)
|
NP_597676.3:p.Val22356Ala
|
|
NM_133437.4:c.67268T>C
(TTN)
|
NP_597681.4:p.Val22423Ala
|
|
NR_038271.1:n.447-23561A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+5378A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.92984T>C
(TTN)
|
XP_011510031.1:p.Val30995Ala
|
|
XM_011511730.1:c.66878T>C
(TTN)
|
XP_011510032.1:p.Val22293Ala
|
|
XM_011511731.1:c.66737T>C
(TTN)
|
XP_011510033.1:p.Val22246Ala
|
|
XM_017004819.1:c.92780T>C
(TTN)
|
XP_016860308.1:p.Val30927Ala
|
|
XM_017004820.1:c.88178T>C
(TTN)
|
XP_016860309.1:p.Val29393Ala
|
|
XM_017004821.1:c.88175T>C
(TTN)
|
XP_016860310.1:p.Val29392Ala
|
|
XM_017004822.1:c.85217T>C
(TTN)
|
XP_016860311.1:p.Val28406Ala
|
|
XM_017004823.1:c.66833T>C
(TTN)
|
XP_016860312.1:p.Val22278Ala
|
|
XM_024453094.1:c.88328T>C
(TTN)
|
XP_024308862.1:p.Val29443Ala
|
|
XM_024453095.1:c.88325T>C
(TTN)
|
XP_024308863.1:p.Val29442Ala
|
|
XM_024453096.1:c.87758T>C
(TTN)
|
XP_024308864.1:p.Val29253Ala
|
|
XM_024453097.1:c.85100T>C
(TTN)
|
XP_024308865.1:p.Val28367Ala
|
|
XM_024453098.1:c.85019T>C
(TTN)
|
XP_024308866.1:p.Val28340Ala
|
|
XM_024453099.1:c.66782T>C
(TTN)
|
XP_024308867.1:p.Val22261Ala
|
|
XM_024453100.1:c.56636T>C
(TTN)
|
XP_024308868.1:p.Val18879Ala
|
|