ENST00000342992.11:c.79842T>C
(TTN)
|
ENSP00000343764.6:p.Thr26614=
|
|
ENST00000342175.11:c.60927T>C
(TTN)
|
ENSP00000340554.6:p.Thr20309=
|
|
ENST00000359218.10:c.60726T>C
(TTN)
|
ENSP00000352154.5:p.Thr20242=
|
|
ENST00000342175.10:c.60927T>C
(TTN)
|
ENSP00000340554.6:p.Thr20309=
|
|
ENST00000342992.10:c.79842T>C
(TTN)
|
ENSP00000343764.6:p.Thr26614=
|
|
ENST00000359218.9:c.60726T>C
(TTN)
|
ENSP00000352154.5:p.Thr20242=
|
|
ENST00000460472.6:c.60351T>C
(TTN)
|
ENSP00000434586.1:p.Thr20117=
|
|
ENST00000589042.5:c.87546T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr29182=
|
|
ENST00000591111.5:c.82623T>C
(TTN)
|
ENSP00000465570.1:p.Thr27541=
|
|
ENST00000615779.4:c.82623T>C
(TTN)
|
ENSP00000483597.1:p.Thr27541=
|
|
NM_001256850.1:c.82623T>C
(TTN)
|
NP_001243779.1:p.Thr27541=
|
|
NM_001267550.2:c.87546T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Thr29182=
|
|
NM_003319.4:c.60351T>C
(TTN)
|
NP_003310.4:p.Thr20117=
|
|
NM_133378.4:c.79842T>C
(TTN)
|
NP_596869.4:p.Thr26614=
|
|
NM_133432.3:c.60726T>C
(TTN)
|
NP_597676.3:p.Thr20242=
|
|
NM_133437.4:c.60927T>C
(TTN)
|
NP_597681.4:p.Thr20309=
|
|
NR_038271.1:n.447-13492A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+15447A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.86643T>C
(TTN)
|
XP_011510031.1:p.Thr28881=
|
|
XM_011511730.1:c.60537T>C
(TTN)
|
XP_011510032.1:p.Thr20179=
|
|
XM_011511731.1:c.60396T>C
(TTN)
|
XP_011510033.1:p.Thr20132=
|
|
XM_017004819.1:c.86439T>C
(TTN)
|
XP_016860308.1:p.Thr28813=
|
|
XM_017004820.1:c.81837T>C
(TTN)
|
XP_016860309.1:p.Thr27279=
|
|
XM_017004821.1:c.81834T>C
(TTN)
|
XP_016860310.1:p.Thr27278=
|
|
XM_017004822.1:c.78876T>C
(TTN)
|
XP_016860311.1:p.Thr26292=
|
|
XM_017004823.1:c.60492T>C
(TTN)
|
XP_016860312.1:p.Thr20164=
|
|
XM_024453094.1:c.81987T>C
(TTN)
|
XP_024308862.1:p.Thr27329=
|
|
XM_024453095.1:c.81984T>C
(TTN)
|
XP_024308863.1:p.Thr27328=
|
|
XM_024453096.1:c.81417T>C
(TTN)
|
XP_024308864.1:p.Thr27139=
|
|
XM_024453097.1:c.78759T>C
(TTN)
|
XP_024308865.1:p.Thr26253=
|
|
XM_024453098.1:c.78678T>C
(TTN)
|
XP_024308866.1:p.Thr26226=
|
|
XM_024453099.1:c.60441T>C
(TTN)
|
XP_024308867.1:p.Thr20147=
|
|
XM_024453100.1:c.50295T>C
(TTN)
|
XP_024308868.1:p.Thr16765=
|
|