ENST00000342992.11:c.69325G>A
(TTN)
|
ENSP00000343764.6:p.Ala23109Thr
|
|
ENST00000342175.11:c.50410G>A
(TTN)
|
ENSP00000340554.6:p.Ala16804Thr
|
|
ENST00000359218.10:c.50209G>A
(TTN)
|
ENSP00000352154.5:p.Ala16737Thr
|
|
ENST00000342175.10:c.50410G>A
(TTN)
|
ENSP00000340554.6:p.Ala16804Thr
|
|
ENST00000342992.10:c.69325G>A
(TTN)
|
ENSP00000343764.6:p.Ala23109Thr
|
|
ENST00000359218.9:c.50209G>A
(TTN)
|
ENSP00000352154.5:p.Ala16737Thr
|
|
ENST00000460472.6:c.49834G>A
(TTN)
|
ENSP00000434586.1:p.Ala16612Thr
|
|
ENST00000589042.5:c.77029G>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ala25677Thr
|
|
ENST00000591111.5:c.72106G>A
(TTN)
|
ENSP00000465570.1:p.Ala24036Thr
|
|
ENST00000615779.4:c.72106G>A
(TTN)
|
ENSP00000483597.1:p.Ala24036Thr
|
|
NM_001256850.1:c.72106G>A
(TTN)
|
NP_001243779.1:p.Ala24036Thr
|
|
NM_001267550.2:c.77029G>A
(TTN)
MANE Select
|
NP_001254479.2:p.Ala25677Thr
|
|
NM_003319.4:c.49834G>A
(TTN)
|
NP_003310.4:p.Ala16612Thr
|
|
NM_133378.4:c.69325G>A
(TTN)
|
NP_596869.4:p.Ala23109Thr
|
|
NM_133432.3:c.50209G>A
(TTN)
|
NP_597676.3:p.Ala16737Thr
|
|
NM_133437.4:c.50410G>A
(TTN)
|
NP_597681.4:p.Ala16804Thr
|
|
NR_038271.1:n.447-2197C>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-13469C>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.76126G>A
(TTN)
|
XP_011510031.1:p.Ala25376Thr
|
|
XM_011511730.1:c.50020G>A
(TTN)
|
XP_011510032.1:p.Ala16674Thr
|
|
XM_011511731.1:c.49879G>A
(TTN)
|
XP_011510033.1:p.Ala16627Thr
|
|
XM_017004819.1:c.75922G>A
(TTN)
|
XP_016860308.1:p.Ala25308Thr
|
|
XM_017004820.1:c.71320G>A
(TTN)
|
XP_016860309.1:p.Ala23774Thr
|
|
XM_017004821.1:c.71317G>A
(TTN)
|
XP_016860310.1:p.Ala23773Thr
|
|
XM_017004822.1:c.68359G>A
(TTN)
|
XP_016860311.1:p.Ala22787Thr
|
|
XM_017004823.1:c.49975G>A
(TTN)
|
XP_016860312.1:p.Ala16659Thr
|
|
XM_024453094.1:c.71470G>A
(TTN)
|
XP_024308862.1:p.Ala23824Thr
|
|
XM_024453095.1:c.71467G>A
(TTN)
|
XP_024308863.1:p.Ala23823Thr
|
|
XM_024453096.1:c.70900G>A
(TTN)
|
XP_024308864.1:p.Ala23634Thr
|
|
XM_024453097.1:c.68242G>A
(TTN)
|
XP_024308865.1:p.Ala22748Thr
|
|
XM_024453098.1:c.68161G>A
(TTN)
|
XP_024308866.1:p.Ala22721Thr
|
|
XM_024453099.1:c.49924G>A
(TTN)
|
XP_024308867.1:p.Ala16642Thr
|
|
XM_024453100.1:c.39778G>A
(TTN)
|
XP_024308868.1:p.Ala13260Thr
|
|