ENST00000342992.11:c.84223G>A
(TTN)
|
ENSP00000343764.6:p.Ala28075Thr
|
|
ENST00000342175.11:c.65308G>A
(TTN)
|
ENSP00000340554.6:p.Ala21770Thr
|
|
ENST00000359218.10:c.65107G>A
(TTN)
|
ENSP00000352154.5:p.Ala21703Thr
|
|
ENST00000342175.10:c.65308G>A
(TTN)
|
ENSP00000340554.6:p.Ala21770Thr
|
|
ENST00000342992.10:c.84223G>A
(TTN)
|
ENSP00000343764.6:p.Ala28075Thr
|
|
ENST00000359218.9:c.65107G>A
(TTN)
|
ENSP00000352154.5:p.Ala21703Thr
|
|
ENST00000460472.6:c.64732G>A
(TTN)
|
ENSP00000434586.1:p.Ala21578Thr
|
|
ENST00000589042.5:c.91927G>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ala30643Thr
|
|
ENST00000591111.5:c.87004G>A
(TTN)
|
ENSP00000465570.1:p.Ala29002Thr
|
|
ENST00000615779.4:c.87004G>A
(TTN)
|
ENSP00000483597.1:p.Ala29002Thr
|
|
NM_001256850.1:c.87004G>A
(TTN)
|
NP_001243779.1:p.Ala29002Thr
|
|
NM_001267550.2:c.91927G>A
(TTN)
MANE Select
|
NP_001254479.2:p.Ala30643Thr
|
|
NM_003319.4:c.64732G>A
(TTN)
|
NP_003310.4:p.Ala21578Thr
|
|
NM_133378.4:c.84223G>A
(TTN)
|
NP_596869.4:p.Ala28075Thr
|
|
NM_133432.3:c.65107G>A
(TTN)
|
NP_597676.3:p.Ala21703Thr
|
|
NM_133437.4:c.65308G>A
(TTN)
|
NP_597681.4:p.Ala21770Thr
|
|
NR_038271.1:n.447-21505C>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+7434C>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.91024G>A
(TTN)
|
XP_011510031.1:p.Ala30342Thr
|
|
XM_011511730.1:c.64918G>A
(TTN)
|
XP_011510032.1:p.Ala21640Thr
|
|
XM_011511731.1:c.64777G>A
(TTN)
|
XP_011510033.1:p.Ala21593Thr
|
|
XM_017004819.1:c.90820G>A
(TTN)
|
XP_016860308.1:p.Ala30274Thr
|
|
XM_017004820.1:c.86218G>A
(TTN)
|
XP_016860309.1:p.Ala28740Thr
|
|
XM_017004821.1:c.86215G>A
(TTN)
|
XP_016860310.1:p.Ala28739Thr
|
|
XM_017004822.1:c.83257G>A
(TTN)
|
XP_016860311.1:p.Ala27753Thr
|
|
XM_017004823.1:c.64873G>A
(TTN)
|
XP_016860312.1:p.Ala21625Thr
|
|
XM_024453094.1:c.86368G>A
(TTN)
|
XP_024308862.1:p.Ala28790Thr
|
|
XM_024453095.1:c.86365G>A
(TTN)
|
XP_024308863.1:p.Ala28789Thr
|
|
XM_024453096.1:c.85798G>A
(TTN)
|
XP_024308864.1:p.Ala28600Thr
|
|
XM_024453097.1:c.83140G>A
(TTN)
|
XP_024308865.1:p.Ala27714Thr
|
|
XM_024453098.1:c.83059G>A
(TTN)
|
XP_024308866.1:p.Ala27687Thr
|
|
XM_024453099.1:c.64822G>A
(TTN)
|
XP_024308867.1:p.Ala21608Thr
|
|
XM_024453100.1:c.54676G>A
(TTN)
|
XP_024308868.1:p.Ala18226Thr
|
|