ENST00000342992.11:c.60831T>A
(TTN)
|
ENSP00000343764.6:p.Pro20277=
|
|
ENST00000342175.11:c.41916T>A
(TTN)
|
ENSP00000340554.6:p.Pro13972=
|
|
ENST00000359218.10:c.41715T>A
(TTN)
|
ENSP00000352154.5:p.Pro13905=
|
|
ENST00000342175.10:c.41916T>A
(TTN)
|
ENSP00000340554.6:p.Pro13972=
|
|
ENST00000342992.10:c.60831T>A
(TTN)
|
ENSP00000343764.6:p.Pro20277=
|
|
ENST00000359218.9:c.41715T>A
(TTN)
|
ENSP00000352154.5:p.Pro13905=
|
|
ENST00000460472.6:c.41340T>A
(TTN)
|
ENSP00000434586.1:p.Pro13780=
|
|
ENST00000589042.5:c.68535T>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Pro22845=
|
|
ENST00000591111.5:c.63612T>A
(TTN)
|
ENSP00000465570.1:p.Pro21204=
|
|
ENST00000615779.4:c.63612T>A
(TTN)
|
ENSP00000483597.1:p.Pro21204=
|
|
NM_001256850.1:c.63612T>A
(TTN)
|
NP_001243779.1:p.Pro21204=
|
|
NM_001267550.2:c.68535T>A
(TTN)
MANE Select
|
NP_001254479.2:p.Pro22845=
|
|
NM_003319.4:c.41340T>A
(TTN)
|
NP_003310.4:p.Pro13780=
|
|
NM_133378.4:c.60831T>A
(TTN)
|
NP_596869.4:p.Pro20277=
|
|
NM_133432.3:c.41715T>A
(TTN)
|
NP_597676.3:p.Pro13905=
|
|
NM_133437.4:c.41916T>A
(TTN)
|
NP_597681.4:p.Pro13972=
|
|
NR_038271.1:n.596+6442A>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-4681A>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.67632T>A
(TTN)
|
XP_011510031.1:p.Pro22544=
|
|
XM_011511730.1:c.41526T>A
(TTN)
|
XP_011510032.1:p.Pro13842=
|
|
XM_011511731.1:c.41385T>A
(TTN)
|
XP_011510033.1:p.Pro13795=
|
|
XM_017004819.1:c.67428T>A
(TTN)
|
XP_016860308.1:p.Pro22476=
|
|
XM_017004820.1:c.62826T>A
(TTN)
|
XP_016860309.1:p.Pro20942=
|
|
XM_017004821.1:c.62823T>A
(TTN)
|
XP_016860310.1:p.Pro20941=
|
|
XM_017004822.1:c.59865T>A
(TTN)
|
XP_016860311.1:p.Pro19955=
|
|
XM_017004823.1:c.41481T>A
(TTN)
|
XP_016860312.1:p.Pro13827=
|
|
XM_024453094.1:c.62976T>A
(TTN)
|
XP_024308862.1:p.Pro20992=
|
|
XM_024453095.1:c.62973T>A
(TTN)
|
XP_024308863.1:p.Pro20991=
|
|
XM_024453096.1:c.62406T>A
(TTN)
|
XP_024308864.1:p.Pro20802=
|
|
XM_024453097.1:c.59748T>A
(TTN)
|
XP_024308865.1:p.Pro19916=
|
|
XM_024453098.1:c.59667T>A
(TTN)
|
XP_024308866.1:p.Pro19889=
|
|
XM_024453099.1:c.41430T>A
(TTN)
|
XP_024308867.1:p.Pro13810=
|
|
XM_024453100.1:c.31284T>A
(TTN)
|
XP_024308868.1:p.Pro10428=
|
|