ENST00000342992.11:c.90382A>G
(TTN)
|
ENSP00000343764.6:p.Thr30128Ala
|
|
ENST00000342175.11:c.71467A>G
(TTN)
|
ENSP00000340554.6:p.Thr23823Ala
|
|
ENST00000359218.10:c.71266A>G
(TTN)
|
ENSP00000352154.5:p.Thr23756Ala
|
|
ENST00000342175.10:c.71467A>G
(TTN)
|
ENSP00000340554.6:p.Thr23823Ala
|
|
ENST00000342992.10:c.90382A>G
(TTN)
|
ENSP00000343764.6:p.Thr30128Ala
|
|
ENST00000359218.9:c.71266A>G
(TTN)
|
ENSP00000352154.5:p.Thr23756Ala
|
|
ENST00000460472.6:c.70891A>G
(TTN)
|
ENSP00000434586.1:p.Thr23631Ala
|
|
ENST00000589042.5:c.98086A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr32696Ala
|
|
ENST00000591111.5:c.93163A>G
(TTN)
|
ENSP00000465570.1:p.Thr31055Ala
|
|
ENST00000615779.4:c.93163A>G
(TTN)
|
ENSP00000483597.1:p.Thr31055Ala
|
|
NM_001256850.1:c.93163A>G
(TTN)
|
NP_001243779.1:p.Thr31055Ala
|
|
NM_001267550.2:c.98086A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Thr32696Ala
|
|
NM_003319.4:c.70891A>G
(TTN)
|
NP_003310.4:p.Thr23631Ala
|
|
NM_133378.4:c.90382A>G
(TTN)
|
NP_596869.4:p.Thr30128Ala
|
|
NM_133432.3:c.71266A>G
(TTN)
|
NP_597676.3:p.Thr23756Ala
|
|
NM_133437.4:c.71467A>G
(TTN)
|
NP_597681.4:p.Thr23823Ala
|
|
NR_038271.1:n.446+16444T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.1841-27T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.97183A>G
(TTN)
|
XP_011510031.1:p.Thr32395Ala
|
|
XM_011511730.1:c.71077A>G
(TTN)
|
XP_011510032.1:p.Thr23693Ala
|
|
XM_011511731.1:c.70936A>G
(TTN)
|
XP_011510033.1:p.Thr23646Ala
|
|
XM_017004819.1:c.96979A>G
(TTN)
|
XP_016860308.1:p.Thr32327Ala
|
|
XM_017004820.1:c.92377A>G
(TTN)
|
XP_016860309.1:p.Thr30793Ala
|
|
XM_017004821.1:c.92374A>G
(TTN)
|
XP_016860310.1:p.Thr30792Ala
|
|
XM_017004822.1:c.89416A>G
(TTN)
|
XP_016860311.1:p.Thr29806Ala
|
|
XM_017004823.1:c.71032A>G
(TTN)
|
XP_016860312.1:p.Thr23678Ala
|
|
XM_024453094.1:c.92527A>G
(TTN)
|
XP_024308862.1:p.Thr30843Ala
|
|
XM_024453095.1:c.92524A>G
(TTN)
|
XP_024308863.1:p.Thr30842Ala
|
|
XM_024453096.1:c.91957A>G
(TTN)
|
XP_024308864.1:p.Thr30653Ala
|
|
XM_024453097.1:c.89299A>G
(TTN)
|
XP_024308865.1:p.Thr29767Ala
|
|
XM_024453098.1:c.89218A>G
(TTN)
|
XP_024308866.1:p.Thr29740Ala
|
|
XM_024453099.1:c.70981A>G
(TTN)
|
XP_024308867.1:p.Thr23661Ala
|
|
XM_024453100.1:c.60835A>G
(TTN)
|
XP_024308868.1:p.Thr20279Ala
|
|