ENST00000342992.11:c.69695T>G
(TTN)
|
ENSP00000343764.6:p.Val23232Gly
|
|
ENST00000342175.11:c.50780T>G
(TTN)
|
ENSP00000340554.6:p.Val16927Gly
|
|
ENST00000359218.10:c.50579T>G
(TTN)
|
ENSP00000352154.5:p.Val16860Gly
|
|
ENST00000342175.10:c.50780T>G
(TTN)
|
ENSP00000340554.6:p.Val16927Gly
|
|
ENST00000342992.10:c.69695T>G
(TTN)
|
ENSP00000343764.6:p.Val23232Gly
|
|
ENST00000359218.9:c.50579T>G
(TTN)
|
ENSP00000352154.5:p.Val16860Gly
|
|
ENST00000460472.6:c.50204T>G
(TTN)
|
ENSP00000434586.1:p.Val16735Gly
|
|
ENST00000589042.5:c.77399T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Val25800Gly
|
|
ENST00000591111.5:c.72476T>G
(TTN)
|
ENSP00000465570.1:p.Val24159Gly
|
|
ENST00000615779.4:c.72476T>G
(TTN)
|
ENSP00000483597.1:p.Val24159Gly
|
|
NM_001256850.1:c.72476T>G
(TTN)
|
NP_001243779.1:p.Val24159Gly
|
|
NM_001267550.2:c.77399T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Val25800Gly
|
|
NM_003319.4:c.50204T>G
(TTN)
|
NP_003310.4:p.Val16735Gly
|
|
NM_133378.4:c.69695T>G
(TTN)
|
NP_596869.4:p.Val23232Gly
|
|
NM_133432.3:c.50579T>G
(TTN)
|
NP_597676.3:p.Val16860Gly
|
|
NM_133437.4:c.50780T>G
(TTN)
|
NP_597681.4:p.Val16927Gly
|
|
NR_038271.1:n.447-2567A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-13839A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.76496T>G
(TTN)
|
XP_011510031.1:p.Val25499Gly
|
|
XM_011511730.1:c.50390T>G
(TTN)
|
XP_011510032.1:p.Val16797Gly
|
|
XM_011511731.1:c.50249T>G
(TTN)
|
XP_011510033.1:p.Val16750Gly
|
|
XM_017004819.1:c.76292T>G
(TTN)
|
XP_016860308.1:p.Val25431Gly
|
|
XM_017004820.1:c.71690T>G
(TTN)
|
XP_016860309.1:p.Val23897Gly
|
|
XM_017004821.1:c.71687T>G
(TTN)
|
XP_016860310.1:p.Val23896Gly
|
|
XM_017004822.1:c.68729T>G
(TTN)
|
XP_016860311.1:p.Val22910Gly
|
|
XM_017004823.1:c.50345T>G
(TTN)
|
XP_016860312.1:p.Val16782Gly
|
|
XM_024453094.1:c.71840T>G
(TTN)
|
XP_024308862.1:p.Val23947Gly
|
|
XM_024453095.1:c.71837T>G
(TTN)
|
XP_024308863.1:p.Val23946Gly
|
|
XM_024453096.1:c.71270T>G
(TTN)
|
XP_024308864.1:p.Val23757Gly
|
|
XM_024453097.1:c.68612T>G
(TTN)
|
XP_024308865.1:p.Val22871Gly
|
|
XM_024453098.1:c.68531T>G
(TTN)
|
XP_024308866.1:p.Val22844Gly
|
|
XM_024453099.1:c.50294T>G
(TTN)
|
XP_024308867.1:p.Val16765Gly
|
|
XM_024453100.1:c.40148T>G
(TTN)
|
XP_024308868.1:p.Val13383Gly
|
|