ENST00000342992.11:c.90384T>C
(TTN)
|
ENSP00000343764.6:p.Thr30128=
|
|
ENST00000342175.11:c.71469T>C
(TTN)
|
ENSP00000340554.6:p.Thr23823=
|
|
ENST00000359218.10:c.71268T>C
(TTN)
|
ENSP00000352154.5:p.Thr23756=
|
|
ENST00000342175.10:c.71469T>C
(TTN)
|
ENSP00000340554.6:p.Thr23823=
|
|
ENST00000342992.10:c.90384T>C
(TTN)
|
ENSP00000343764.6:p.Thr30128=
|
|
ENST00000359218.9:c.71268T>C
(TTN)
|
ENSP00000352154.5:p.Thr23756=
|
|
ENST00000460472.6:c.70893T>C
(TTN)
|
ENSP00000434586.1:p.Thr23631=
|
|
ENST00000589042.5:c.98088T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr32696=
|
|
ENST00000591111.5:c.93165T>C
(TTN)
|
ENSP00000465570.1:p.Thr31055=
|
|
ENST00000615779.4:c.93165T>C
(TTN)
|
ENSP00000483597.1:p.Thr31055=
|
|
NM_001256850.1:c.93165T>C
(TTN)
|
NP_001243779.1:p.Thr31055=
|
|
NM_001267550.2:c.98088T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Thr32696=
|
|
NM_003319.4:c.70893T>C
(TTN)
|
NP_003310.4:p.Thr23631=
|
|
NM_133378.4:c.90384T>C
(TTN)
|
NP_596869.4:p.Thr30128=
|
|
NM_133432.3:c.71268T>C
(TTN)
|
NP_597676.3:p.Thr23756=
|
|
NM_133437.4:c.71469T>C
(TTN)
|
NP_597681.4:p.Thr23823=
|
|
NR_038271.1:n.446+16442A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.1841-29A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.97185T>C
(TTN)
|
XP_011510031.1:p.Thr32395=
|
|
XM_011511730.1:c.71079T>C
(TTN)
|
XP_011510032.1:p.Thr23693=
|
|
XM_011511731.1:c.70938T>C
(TTN)
|
XP_011510033.1:p.Thr23646=
|
|
XM_017004819.1:c.96981T>C
(TTN)
|
XP_016860308.1:p.Thr32327=
|
|
XM_017004820.1:c.92379T>C
(TTN)
|
XP_016860309.1:p.Thr30793=
|
|
XM_017004821.1:c.92376T>C
(TTN)
|
XP_016860310.1:p.Thr30792=
|
|
XM_017004822.1:c.89418T>C
(TTN)
|
XP_016860311.1:p.Thr29806=
|
|
XM_017004823.1:c.71034T>C
(TTN)
|
XP_016860312.1:p.Thr23678=
|
|
XM_024453094.1:c.92529T>C
(TTN)
|
XP_024308862.1:p.Thr30843=
|
|
XM_024453095.1:c.92526T>C
(TTN)
|
XP_024308863.1:p.Thr30842=
|
|
XM_024453096.1:c.91959T>C
(TTN)
|
XP_024308864.1:p.Thr30653=
|
|
XM_024453097.1:c.89301T>C
(TTN)
|
XP_024308865.1:p.Thr29767=
|
|
XM_024453098.1:c.89220T>C
(TTN)
|
XP_024308866.1:p.Thr29740=
|
|
XM_024453099.1:c.70983T>C
(TTN)
|
XP_024308867.1:p.Thr23661=
|
|
XM_024453100.1:c.60837T>C
(TTN)
|
XP_024308868.1:p.Thr20279=
|
|