ENST00000342992.11:c.91867C>T
(TTN)
|
ENSP00000343764.6:p.Gln30623Ter
|
|
ENST00000342175.11:c.72952C>T
(TTN)
|
ENSP00000340554.6:p.Gln24318Ter
|
|
ENST00000359218.10:c.72751C>T
(TTN)
|
ENSP00000352154.5:p.Gln24251Ter
|
|
ENST00000342175.10:c.72952C>T
(TTN)
|
ENSP00000340554.6:p.Gln24318Ter
|
|
ENST00000342992.10:c.91867C>T
(TTN)
|
ENSP00000343764.6:p.Gln30623Ter
|
|
ENST00000359218.9:c.72751C>T
(TTN)
|
ENSP00000352154.5:p.Gln24251Ter
|
|
ENST00000460472.6:c.72376C>T
(TTN)
|
ENSP00000434586.1:p.Gln24126Ter
|
|
ENST00000589042.5:c.99571C>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gln33191Ter
|
|
ENST00000591111.5:c.94648C>T
(TTN)
|
ENSP00000465570.1:p.Gln31550Ter
|
|
ENST00000615779.4:c.94648C>T
(TTN)
|
ENSP00000483597.1:p.Gln31550Ter
|
|
NM_001256850.1:c.94648C>T
(TTN)
|
NP_001243779.1:p.Gln31550Ter
|
|
NM_001267550.2:c.99571C>T
(TTN)
MANE Select
|
NP_001254479.2:p.Gln33191Ter
|
|
NM_003319.4:c.72376C>T
(TTN)
|
NP_003310.4:p.Gln24126Ter
|
|
NM_133378.4:c.91867C>T
(TTN)
|
NP_596869.4:p.Gln30623Ter
|
|
NM_133432.3:c.72751C>T
(TTN)
|
NP_597676.3:p.Gln24251Ter
|
|
NM_133437.4:c.72952C>T
(TTN)
|
NP_597681.4:p.Gln24318Ter
|
|
NR_038271.1:n.446+14000G>A
(TTN-AS1)
|
|
|
NR_038272.1:n.592G>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.98668C>T
(TTN)
|
XP_011510031.1:p.Gln32890Ter
|
|
XM_011511730.1:c.72562C>T
(TTN)
|
XP_011510032.1:p.Gln24188Ter
|
|
XM_011511731.1:c.72421C>T
(TTN)
|
XP_011510033.1:p.Gln24141Ter
|
|
XM_017004819.1:c.98464C>T
(TTN)
|
XP_016860308.1:p.Gln32822Ter
|
|
XM_017004820.1:c.93862C>T
(TTN)
|
XP_016860309.1:p.Gln31288Ter
|
|
XM_017004821.1:c.93859C>T
(TTN)
|
XP_016860310.1:p.Gln31287Ter
|
|
XM_017004822.1:c.90901C>T
(TTN)
|
XP_016860311.1:p.Gln30301Ter
|
|
XM_017004823.1:c.72517C>T
(TTN)
|
XP_016860312.1:p.Gln24173Ter
|
|
XM_024453094.1:c.94012C>T
(TTN)
|
XP_024308862.1:p.Gln31338Ter
|
|
XM_024453095.1:c.94009C>T
(TTN)
|
XP_024308863.1:p.Gln31337Ter
|
|
XM_024453096.1:c.93442C>T
(TTN)
|
XP_024308864.1:p.Gln31148Ter
|
|
XM_024453097.1:c.90784C>T
(TTN)
|
XP_024308865.1:p.Gln30262Ter
|
|
XM_024453098.1:c.90703C>T
(TTN)
|
XP_024308866.1:p.Gln30235Ter
|
|
XM_024453099.1:c.72466C>T
(TTN)
|
XP_024308867.1:p.Gln24156Ter
|
|
XM_024453100.1:c.62320C>T
(TTN)
|
XP_024308868.1:p.Gln20774Ter
|
|