ENST00000342992.11:c.67886T>C
(TTN)
|
ENSP00000343764.6:p.Val22629Ala
|
|
ENST00000342175.11:c.48971T>C
(TTN)
|
ENSP00000340554.6:p.Val16324Ala
|
|
ENST00000359218.10:c.48770T>C
(TTN)
|
ENSP00000352154.5:p.Val16257Ala
|
|
ENST00000342175.10:c.48971T>C
(TTN)
|
ENSP00000340554.6:p.Val16324Ala
|
|
ENST00000342992.10:c.67886T>C
(TTN)
|
ENSP00000343764.6:p.Val22629Ala
|
|
ENST00000359218.9:c.48770T>C
(TTN)
|
ENSP00000352154.5:p.Val16257Ala
|
|
ENST00000460472.6:c.48395T>C
(TTN)
|
ENSP00000434586.1:p.Val16132Ala
|
|
ENST00000589042.5:c.75590T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Val25197Ala
|
|
ENST00000591111.5:c.70667T>C
(TTN)
|
ENSP00000465570.1:p.Val23556Ala
|
|
ENST00000615779.4:c.70667T>C
(TTN)
|
ENSP00000483597.1:p.Val23556Ala
|
|
NM_001256850.1:c.70667T>C
(TTN)
|
NP_001243779.1:p.Val23556Ala
|
|
NM_001267550.2:c.75590T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Val25197Ala
|
|
NM_003319.4:c.48395T>C
(TTN)
|
NP_003310.4:p.Val16132Ala
|
|
NM_133378.4:c.67886T>C
(TTN)
|
NP_596869.4:p.Val22629Ala
|
|
NM_133432.3:c.48770T>C
(TTN)
|
NP_597676.3:p.Val16257Ala
|
|
NM_133437.4:c.48971T>C
(TTN)
|
NP_597681.4:p.Val16324Ala
|
|
NR_038271.1:n.447-758A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-12030A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.74687T>C
(TTN)
|
XP_011510031.1:p.Val24896Ala
|
|
XM_011511730.1:c.48581T>C
(TTN)
|
XP_011510032.1:p.Val16194Ala
|
|
XM_011511731.1:c.48440T>C
(TTN)
|
XP_011510033.1:p.Val16147Ala
|
|
XM_017004819.1:c.74483T>C
(TTN)
|
XP_016860308.1:p.Val24828Ala
|
|
XM_017004820.1:c.69881T>C
(TTN)
|
XP_016860309.1:p.Val23294Ala
|
|
XM_017004821.1:c.69878T>C
(TTN)
|
XP_016860310.1:p.Val23293Ala
|
|
XM_017004822.1:c.66920T>C
(TTN)
|
XP_016860311.1:p.Val22307Ala
|
|
XM_017004823.1:c.48536T>C
(TTN)
|
XP_016860312.1:p.Val16179Ala
|
|
XM_024453094.1:c.70031T>C
(TTN)
|
XP_024308862.1:p.Val23344Ala
|
|
XM_024453095.1:c.70028T>C
(TTN)
|
XP_024308863.1:p.Val23343Ala
|
|
XM_024453096.1:c.69461T>C
(TTN)
|
XP_024308864.1:p.Val23154Ala
|
|
XM_024453097.1:c.66803T>C
(TTN)
|
XP_024308865.1:p.Val22268Ala
|
|
XM_024453098.1:c.66722T>C
(TTN)
|
XP_024308866.1:p.Val22241Ala
|
|
XM_024453099.1:c.48485T>C
(TTN)
|
XP_024308867.1:p.Val16162Ala
|
|
XM_024453100.1:c.38339T>C
(TTN)
|
XP_024308868.1:p.Val12780Ala
|
|