ENST00000342992.11:c.98276A>T
(TTN)
|
ENSP00000343764.6:p.Lys32759Met
|
|
ENST00000342175.11:c.79361A>T
(TTN)
|
ENSP00000340554.6:p.Lys26454Met
|
|
ENST00000359218.10:c.79160A>T
(TTN)
|
ENSP00000352154.5:p.Lys26387Met
|
|
ENST00000342175.10:c.79361A>T
(TTN)
|
ENSP00000340554.6:p.Lys26454Met
|
|
ENST00000342992.10:c.98276A>T
(TTN)
|
ENSP00000343764.6:p.Lys32759Met
|
|
ENST00000359218.9:c.79160A>T
(TTN)
|
ENSP00000352154.5:p.Lys26387Met
|
|
ENST00000460472.6:c.78785A>T
(TTN)
|
ENSP00000434586.1:p.Lys26262Met
|
|
ENST00000589042.5:c.105980A>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Lys35327Met
|
|
ENST00000591111.5:c.101057A>T
(TTN)
|
ENSP00000465570.1:p.Lys33686Met
|
|
ENST00000615779.4:c.101057A>T
(TTN)
|
ENSP00000483597.1:p.Lys33686Met
|
|
NM_001256850.1:c.101057A>T
(TTN)
|
NP_001243779.1:p.Lys33686Met
|
|
NM_001267550.2:c.105980A>T
(TTN)
MANE Select
|
NP_001254479.2:p.Lys35327Met
|
|
NM_003319.4:c.78785A>T
(TTN)
|
NP_003310.4:p.Lys26262Met
|
|
NM_133378.4:c.98276A>T
(TTN)
|
NP_596869.4:p.Lys32759Met
|
|
NM_133432.3:c.79160A>T
(TTN)
|
NP_597676.3:p.Lys26387Met
|
|
NM_133437.4:c.79361A>T
(TTN)
|
NP_597681.4:p.Lys26454Met
|
|
NR_038271.1:n.446+6999T>A
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5097T>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.105077A>T
(TTN)
|
XP_011510031.1:p.Lys35026Met
|
|
XM_011511730.1:c.78971A>T
(TTN)
|
XP_011510032.1:p.Lys26324Met
|
|
XM_011511731.1:c.78830A>T
(TTN)
|
XP_011510033.1:p.Lys26277Met
|
|
XM_017004819.1:c.104873A>T
(TTN)
|
XP_016860308.1:p.Lys34958Met
|
|
XM_017004820.1:c.100271A>T
(TTN)
|
XP_016860309.1:p.Lys33424Met
|
|
XM_017004821.1:c.100268A>T
(TTN)
|
XP_016860310.1:p.Lys33423Met
|
|
XM_017004822.1:c.97310A>T
(TTN)
|
XP_016860311.1:p.Lys32437Met
|
|
XM_017004823.1:c.78926A>T
(TTN)
|
XP_016860312.1:p.Lys26309Met
|
|
XM_024453094.1:c.100421A>T
(TTN)
|
XP_024308862.1:p.Lys33474Met
|
|
XM_024453095.1:c.100418A>T
(TTN)
|
XP_024308863.1:p.Lys33473Met
|
|
XM_024453096.1:c.99851A>T
(TTN)
|
XP_024308864.1:p.Lys33284Met
|
|
XM_024453097.1:c.97193A>T
(TTN)
|
XP_024308865.1:p.Lys32398Met
|
|
XM_024453098.1:c.97112A>T
(TTN)
|
XP_024308866.1:p.Lys32371Met
|
|
XM_024453099.1:c.78875A>T
(TTN)
|
XP_024308867.1:p.Lys26292Met
|
|
XM_024453100.1:c.68729A>T
(TTN)
|
XP_024308868.1:p.Lys22910Met
|
|