ENST00000342992.11:c.87414T>G
(TTN)
|
ENSP00000343764.6:p.Leu29138=
|
|
ENST00000342175.11:c.68499T>G
(TTN)
|
ENSP00000340554.6:p.Leu22833=
|
|
ENST00000359218.10:c.68298T>G
(TTN)
|
ENSP00000352154.5:p.Leu22766=
|
|
ENST00000342175.10:c.68499T>G
(TTN)
|
ENSP00000340554.6:p.Leu22833=
|
|
ENST00000342992.10:c.87414T>G
(TTN)
|
ENSP00000343764.6:p.Leu29138=
|
|
ENST00000359218.9:c.68298T>G
(TTN)
|
ENSP00000352154.5:p.Leu22766=
|
|
ENST00000460472.6:c.67923T>G
(TTN)
|
ENSP00000434586.1:p.Leu22641=
|
|
ENST00000589042.5:c.95118T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu31706=
|
|
ENST00000591111.5:c.90195T>G
(TTN)
|
ENSP00000465570.1:p.Leu30065=
|
|
ENST00000615779.4:c.90195T>G
(TTN)
|
ENSP00000483597.1:p.Leu30065=
|
|
NM_001256850.1:c.90195T>G
(TTN)
|
NP_001243779.1:p.Leu30065=
|
|
NM_001267550.2:c.95118T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Leu31706=
|
|
NM_003319.4:c.67923T>G
(TTN)
|
NP_003310.4:p.Leu22641=
|
|
NM_133378.4:c.87414T>G
(TTN)
|
NP_596869.4:p.Leu29138=
|
|
NM_133432.3:c.68298T>G
(TTN)
|
NP_597676.3:p.Leu22766=
|
|
NM_133437.4:c.68499T>G
(TTN)
|
NP_597681.4:p.Leu22833=
|
|
NR_038271.1:n.446+22577A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+3852A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.94215T>G
(TTN)
|
XP_011510031.1:p.Leu31405=
|
|
XM_011511730.1:c.68109T>G
(TTN)
|
XP_011510032.1:p.Leu22703=
|
|
XM_011511731.1:c.67968T>G
(TTN)
|
XP_011510033.1:p.Leu22656=
|
|
XM_017004819.1:c.94011T>G
(TTN)
|
XP_016860308.1:p.Leu31337=
|
|
XM_017004820.1:c.89409T>G
(TTN)
|
XP_016860309.1:p.Leu29803=
|
|
XM_017004821.1:c.89406T>G
(TTN)
|
XP_016860310.1:p.Leu29802=
|
|
XM_017004822.1:c.86448T>G
(TTN)
|
XP_016860311.1:p.Leu28816=
|
|
XM_017004823.1:c.68064T>G
(TTN)
|
XP_016860312.1:p.Leu22688=
|
|
XM_024453094.1:c.89559T>G
(TTN)
|
XP_024308862.1:p.Leu29853=
|
|
XM_024453095.1:c.89556T>G
(TTN)
|
XP_024308863.1:p.Leu29852=
|
|
XM_024453096.1:c.88989T>G
(TTN)
|
XP_024308864.1:p.Leu29663=
|
|
XM_024453097.1:c.86331T>G
(TTN)
|
XP_024308865.1:p.Leu28777=
|
|
XM_024453098.1:c.86250T>G
(TTN)
|
XP_024308866.1:p.Leu28750=
|
|
XM_024453099.1:c.68013T>G
(TTN)
|
XP_024308867.1:p.Leu22671=
|
|
XM_024453100.1:c.57867T>G
(TTN)
|
XP_024308868.1:p.Leu19289=
|
|