ENST00000342992.11:c.78679C>G
(TTN)
|
ENSP00000343764.6:p.Leu26227Val
|
|
ENST00000342175.11:c.59764C>G
(TTN)
|
ENSP00000340554.6:p.Leu19922Val
|
|
ENST00000359218.10:c.59563C>G
(TTN)
|
ENSP00000352154.5:p.Leu19855Val
|
|
ENST00000342175.10:c.59764C>G
(TTN)
|
ENSP00000340554.6:p.Leu19922Val
|
|
ENST00000342992.10:c.78679C>G
(TTN)
|
ENSP00000343764.6:p.Leu26227Val
|
|
ENST00000359218.9:c.59563C>G
(TTN)
|
ENSP00000352154.5:p.Leu19855Val
|
|
ENST00000460472.6:c.59188C>G
(TTN)
|
ENSP00000434586.1:p.Leu19730Val
|
|
ENST00000589042.5:c.86383C>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu28795Val
|
|
ENST00000591111.5:c.81460C>G
(TTN)
|
ENSP00000465570.1:p.Leu27154Val
|
|
ENST00000615779.4:c.81460C>G
(TTN)
|
ENSP00000483597.1:p.Leu27154Val
|
|
NM_001256850.1:c.81460C>G
(TTN)
|
NP_001243779.1:p.Leu27154Val
|
|
NM_001267550.2:c.86383C>G
(TTN)
MANE Select
|
NP_001254479.2:p.Leu28795Val
|
|
NM_003319.4:c.59188C>G
(TTN)
|
NP_003310.4:p.Leu19730Val
|
|
NM_133378.4:c.78679C>G
(TTN)
|
NP_596869.4:p.Leu26227Val
|
|
NM_133432.3:c.59563C>G
(TTN)
|
NP_597676.3:p.Leu19855Val
|
|
NM_133437.4:c.59764C>G
(TTN)
|
NP_597681.4:p.Leu19922Val
|
|
NR_038271.1:n.447-11551G>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+17388G>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.85480C>G
(TTN)
|
XP_011510031.1:p.Leu28494Val
|
|
XM_011511730.1:c.59374C>G
(TTN)
|
XP_011510032.1:p.Leu19792Val
|
|
XM_011511731.1:c.59233C>G
(TTN)
|
XP_011510033.1:p.Leu19745Val
|
|
XM_017004819.1:c.85276C>G
(TTN)
|
XP_016860308.1:p.Leu28426Val
|
|
XM_017004820.1:c.80674C>G
(TTN)
|
XP_016860309.1:p.Leu26892Val
|
|
XM_017004821.1:c.80671C>G
(TTN)
|
XP_016860310.1:p.Leu26891Val
|
|
XM_017004822.1:c.77713C>G
(TTN)
|
XP_016860311.1:p.Leu25905Val
|
|
XM_017004823.1:c.59329C>G
(TTN)
|
XP_016860312.1:p.Leu19777Val
|
|
XM_024453094.1:c.80824C>G
(TTN)
|
XP_024308862.1:p.Leu26942Val
|
|
XM_024453095.1:c.80821C>G
(TTN)
|
XP_024308863.1:p.Leu26941Val
|
|
XM_024453096.1:c.80254C>G
(TTN)
|
XP_024308864.1:p.Leu26752Val
|
|
XM_024453097.1:c.77596C>G
(TTN)
|
XP_024308865.1:p.Leu25866Val
|
|
XM_024453098.1:c.77515C>G
(TTN)
|
XP_024308866.1:p.Leu25839Val
|
|
XM_024453099.1:c.59278C>G
(TTN)
|
XP_024308867.1:p.Leu19760Val
|
|
XM_024453100.1:c.49132C>G
(TTN)
|
XP_024308868.1:p.Leu16378Val
|
|