ENST00000342992.11:c.59930T>G
(TTN)
|
ENSP00000343764.6:p.Val19977Gly
|
|
ENST00000342175.11:c.41015T>G
(TTN)
|
ENSP00000340554.6:p.Val13672Gly
|
|
ENST00000359218.10:c.40814T>G
(TTN)
|
ENSP00000352154.5:p.Val13605Gly
|
|
ENST00000342175.10:c.41015T>G
(TTN)
|
ENSP00000340554.6:p.Val13672Gly
|
|
ENST00000342992.10:c.59930T>G
(TTN)
|
ENSP00000343764.6:p.Val19977Gly
|
|
ENST00000359218.9:c.40814T>G
(TTN)
|
ENSP00000352154.5:p.Val13605Gly
|
|
ENST00000460472.6:c.40439T>G
(TTN)
|
ENSP00000434586.1:p.Val13480Gly
|
|
ENST00000589042.5:c.67634T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Val22545Gly
|
|
ENST00000591111.5:c.62711T>G
(TTN)
|
ENSP00000465570.1:p.Val20904Gly
|
|
ENST00000615779.4:c.62711T>G
(TTN)
|
ENSP00000483597.1:p.Val20904Gly
|
|
NM_001256850.1:c.62711T>G
(TTN)
|
NP_001243779.1:p.Val20904Gly
|
|
NM_001267550.2:c.67634T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Val22545Gly
|
|
NM_003319.4:c.40439T>G
(TTN)
|
NP_003310.4:p.Val13480Gly
|
|
NM_133378.4:c.59930T>G
(TTN)
|
NP_596869.4:p.Val19977Gly
|
|
NM_133432.3:c.40814T>G
(TTN)
|
NP_597676.3:p.Val13605Gly
|
|
NM_133437.4:c.41015T>G
(TTN)
|
NP_597681.4:p.Val13672Gly
|
|
NR_038271.1:n.596+8114A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-3009A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.66731T>G
(TTN)
|
XP_011510031.1:p.Val22244Gly
|
|
XM_011511730.1:c.40625T>G
(TTN)
|
XP_011510032.1:p.Val13542Gly
|
|
XM_011511731.1:c.40484T>G
(TTN)
|
XP_011510033.1:p.Val13495Gly
|
|
XM_017004819.1:c.66527T>G
(TTN)
|
XP_016860308.1:p.Val22176Gly
|
|
XM_017004820.1:c.61925T>G
(TTN)
|
XP_016860309.1:p.Val20642Gly
|
|
XM_017004821.1:c.61922T>G
(TTN)
|
XP_016860310.1:p.Val20641Gly
|
|
XM_017004822.1:c.58964T>G
(TTN)
|
XP_016860311.1:p.Val19655Gly
|
|
XM_017004823.1:c.40580T>G
(TTN)
|
XP_016860312.1:p.Val13527Gly
|
|
XM_024453094.1:c.62075T>G
(TTN)
|
XP_024308862.1:p.Val20692Gly
|
|
XM_024453095.1:c.62072T>G
(TTN)
|
XP_024308863.1:p.Val20691Gly
|
|
XM_024453096.1:c.61505T>G
(TTN)
|
XP_024308864.1:p.Val20502Gly
|
|
XM_024453097.1:c.58847T>G
(TTN)
|
XP_024308865.1:p.Val19616Gly
|
|
XM_024453098.1:c.58766T>G
(TTN)
|
XP_024308866.1:p.Val19589Gly
|
|
XM_024453099.1:c.40529T>G
(TTN)
|
XP_024308867.1:p.Val13510Gly
|
|
XM_024453100.1:c.30383T>G
(TTN)
|
XP_024308868.1:p.Val10128Gly
|
|