ENST00000342992.11:c.79937C>G
(TTN)
|
ENSP00000343764.6:p.Ala26646Gly
|
|
ENST00000342175.11:c.61022C>G
(TTN)
|
ENSP00000340554.6:p.Ala20341Gly
|
|
ENST00000359218.10:c.60821C>G
(TTN)
|
ENSP00000352154.5:p.Ala20274Gly
|
|
ENST00000342175.10:c.61022C>G
(TTN)
|
ENSP00000340554.6:p.Ala20341Gly
|
|
ENST00000342992.10:c.79937C>G
(TTN)
|
ENSP00000343764.6:p.Ala26646Gly
|
|
ENST00000359218.9:c.60821C>G
(TTN)
|
ENSP00000352154.5:p.Ala20274Gly
|
|
ENST00000460472.6:c.60446C>G
(TTN)
|
ENSP00000434586.1:p.Ala20149Gly
|
|
ENST00000589042.5:c.87641C>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ala29214Gly
|
|
ENST00000591111.5:c.82718C>G
(TTN)
|
ENSP00000465570.1:p.Ala27573Gly
|
|
ENST00000615779.4:c.82718C>G
(TTN)
|
ENSP00000483597.1:p.Ala27573Gly
|
|
NM_001256850.1:c.82718C>G
(TTN)
|
NP_001243779.1:p.Ala27573Gly
|
|
NM_001267550.2:c.87641C>G
(TTN)
MANE Select
|
NP_001254479.2:p.Ala29214Gly
|
|
NM_003319.4:c.60446C>G
(TTN)
|
NP_003310.4:p.Ala20149Gly
|
|
NM_133378.4:c.79937C>G
(TTN)
|
NP_596869.4:p.Ala26646Gly
|
|
NM_133432.3:c.60821C>G
(TTN)
|
NP_597676.3:p.Ala20274Gly
|
|
NM_133437.4:c.61022C>G
(TTN)
|
NP_597681.4:p.Ala20341Gly
|
|
NR_038271.1:n.447-13587G>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+15352G>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.86738C>G
(TTN)
|
XP_011510031.1:p.Ala28913Gly
|
|
XM_011511730.1:c.60632C>G
(TTN)
|
XP_011510032.1:p.Ala20211Gly
|
|
XM_011511731.1:c.60491C>G
(TTN)
|
XP_011510033.1:p.Ala20164Gly
|
|
XM_017004819.1:c.86534C>G
(TTN)
|
XP_016860308.1:p.Ala28845Gly
|
|
XM_017004820.1:c.81932C>G
(TTN)
|
XP_016860309.1:p.Ala27311Gly
|
|
XM_017004821.1:c.81929C>G
(TTN)
|
XP_016860310.1:p.Ala27310Gly
|
|
XM_017004822.1:c.78971C>G
(TTN)
|
XP_016860311.1:p.Ala26324Gly
|
|
XM_017004823.1:c.60587C>G
(TTN)
|
XP_016860312.1:p.Ala20196Gly
|
|
XM_024453094.1:c.82082C>G
(TTN)
|
XP_024308862.1:p.Ala27361Gly
|
|
XM_024453095.1:c.82079C>G
(TTN)
|
XP_024308863.1:p.Ala27360Gly
|
|
XM_024453096.1:c.81512C>G
(TTN)
|
XP_024308864.1:p.Ala27171Gly
|
|
XM_024453097.1:c.78854C>G
(TTN)
|
XP_024308865.1:p.Ala26285Gly
|
|
XM_024453098.1:c.78773C>G
(TTN)
|
XP_024308866.1:p.Ala26258Gly
|
|
XM_024453099.1:c.60536C>G
(TTN)
|
XP_024308867.1:p.Ala20179Gly
|
|
XM_024453100.1:c.50390C>G
(TTN)
|
XP_024308868.1:p.Ala16797Gly
|
|