ENST00000342992.11:c.62340C>T
(TTN)
|
ENSP00000343764.6:p.Ala20780=
|
|
ENST00000342175.11:c.43425C>T
(TTN)
|
ENSP00000340554.6:p.Ala14475=
|
|
ENST00000359218.10:c.43224C>T
(TTN)
|
ENSP00000352154.5:p.Ala14408=
|
|
ENST00000342175.10:c.43425C>T
(TTN)
|
ENSP00000340554.6:p.Ala14475=
|
|
ENST00000342992.10:c.62340C>T
(TTN)
|
ENSP00000343764.6:p.Ala20780=
|
|
ENST00000359218.9:c.43224C>T
(TTN)
|
ENSP00000352154.5:p.Ala14408=
|
|
ENST00000460472.6:c.42849C>T
(TTN)
|
ENSP00000434586.1:p.Ala14283=
|
|
ENST00000589042.5:c.70044C>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ala23348=
|
|
ENST00000591111.5:c.65121C>T
(TTN)
|
ENSP00000465570.1:p.Ala21707=
|
|
ENST00000615779.4:c.65121C>T
(TTN)
|
ENSP00000483597.1:p.Ala21707=
|
|
NM_001256850.1:c.65121C>T
(TTN)
|
NP_001243779.1:p.Ala21707=
|
|
NM_001267550.2:c.70044C>T
(TTN)
MANE Select
|
NP_001254479.2:p.Ala23348=
|
|
NM_003319.4:c.42849C>T
(TTN)
|
NP_003310.4:p.Ala14283=
|
|
NM_133378.4:c.62340C>T
(TTN)
|
NP_596869.4:p.Ala20780=
|
|
NM_133432.3:c.43224C>T
(TTN)
|
NP_597676.3:p.Ala14408=
|
|
NM_133437.4:c.43425C>T
(TTN)
|
NP_597681.4:p.Ala14475=
|
|
NR_038271.1:n.596+4639G>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-6484G>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.69141C>T
(TTN)
|
XP_011510031.1:p.Ala23047=
|
|
XM_011511730.1:c.43035C>T
(TTN)
|
XP_011510032.1:p.Ala14345=
|
|
XM_011511731.1:c.42894C>T
(TTN)
|
XP_011510033.1:p.Ala14298=
|
|
XM_017004819.1:c.68937C>T
(TTN)
|
XP_016860308.1:p.Ala22979=
|
|
XM_017004820.1:c.64335C>T
(TTN)
|
XP_016860309.1:p.Ala21445=
|
|
XM_017004821.1:c.64332C>T
(TTN)
|
XP_016860310.1:p.Ala21444=
|
|
XM_017004822.1:c.61374C>T
(TTN)
|
XP_016860311.1:p.Ala20458=
|
|
XM_017004823.1:c.42990C>T
(TTN)
|
XP_016860312.1:p.Ala14330=
|
|
XM_024453094.1:c.64485C>T
(TTN)
|
XP_024308862.1:p.Ala21495=
|
|
XM_024453095.1:c.64482C>T
(TTN)
|
XP_024308863.1:p.Ala21494=
|
|
XM_024453096.1:c.63915C>T
(TTN)
|
XP_024308864.1:p.Ala21305=
|
|
XM_024453097.1:c.61257C>T
(TTN)
|
XP_024308865.1:p.Ala20419=
|
|
XM_024453098.1:c.61176C>T
(TTN)
|
XP_024308866.1:p.Ala20392=
|
|
XM_024453099.1:c.42939C>T
(TTN)
|
XP_024308867.1:p.Ala14313=
|
|
XM_024453100.1:c.32793C>T
(TTN)
|
XP_024308868.1:p.Ala10931=
|
|