ENST00000342992.11:c.98748T>C
(TTN)
|
ENSP00000343764.6:p.Thr32916=
|
|
ENST00000342175.11:c.79833T>C
(TTN)
|
ENSP00000340554.6:p.Thr26611=
|
|
ENST00000359218.10:c.79632T>C
(TTN)
|
ENSP00000352154.5:p.Thr26544=
|
|
ENST00000342175.10:c.79833T>C
(TTN)
|
ENSP00000340554.6:p.Thr26611=
|
|
ENST00000342992.10:c.98748T>C
(TTN)
|
ENSP00000343764.6:p.Thr32916=
|
|
ENST00000359218.9:c.79632T>C
(TTN)
|
ENSP00000352154.5:p.Thr26544=
|
|
ENST00000460472.6:c.79257T>C
(TTN)
|
ENSP00000434586.1:p.Thr26419=
|
|
ENST00000589042.5:c.106452T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr35484=
|
|
ENST00000591111.5:c.101529T>C
(TTN)
|
ENSP00000465570.1:p.Thr33843=
|
|
ENST00000615779.4:c.101529T>C
(TTN)
|
ENSP00000483597.1:p.Thr33843=
|
|
NM_001256850.1:c.101529T>C
(TTN)
|
NP_001243779.1:p.Thr33843=
|
|
NM_001267550.2:c.106452T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Thr35484=
|
|
NM_003319.4:c.79257T>C
(TTN)
|
NP_003310.4:p.Thr26419=
|
|
NM_133378.4:c.98748T>C
(TTN)
|
NP_596869.4:p.Thr32916=
|
|
NM_133432.3:c.79632T>C
(TTN)
|
NP_597676.3:p.Thr26544=
|
|
NM_133437.4:c.79833T>C
(TTN)
|
NP_597681.4:p.Thr26611=
|
|
NR_038271.1:n.446+6403A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5693A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.105549T>C
(TTN)
|
XP_011510031.1:p.Thr35183=
|
|
XM_011511730.1:c.79443T>C
(TTN)
|
XP_011510032.1:p.Thr26481=
|
|
XM_011511731.1:c.79302T>C
(TTN)
|
XP_011510033.1:p.Thr26434=
|
|
XM_017004819.1:c.105345T>C
(TTN)
|
XP_016860308.1:p.Thr35115=
|
|
XM_017004820.1:c.100743T>C
(TTN)
|
XP_016860309.1:p.Thr33581=
|
|
XM_017004821.1:c.100740T>C
(TTN)
|
XP_016860310.1:p.Thr33580=
|
|
XM_017004822.1:c.97782T>C
(TTN)
|
XP_016860311.1:p.Thr32594=
|
|
XM_017004823.1:c.79398T>C
(TTN)
|
XP_016860312.1:p.Thr26466=
|
|
XM_024453094.1:c.100893T>C
(TTN)
|
XP_024308862.1:p.Thr33631=
|
|
XM_024453095.1:c.100890T>C
(TTN)
|
XP_024308863.1:p.Thr33630=
|
|
XM_024453096.1:c.100323T>C
(TTN)
|
XP_024308864.1:p.Thr33441=
|
|
XM_024453097.1:c.97665T>C
(TTN)
|
XP_024308865.1:p.Thr32555=
|
|
XM_024453098.1:c.97584T>C
(TTN)
|
XP_024308866.1:p.Thr32528=
|
|
XM_024453099.1:c.79347T>C
(TTN)
|
XP_024308867.1:p.Thr26449=
|
|
XM_024453100.1:c.69201T>C
(TTN)
|
XP_024308868.1:p.Thr23067=
|
|