ENST00000342992.11:c.78681C>A
(TTN)
|
ENSP00000343764.6:p.Leu26227=
|
|
ENST00000342175.11:c.59766C>A
(TTN)
|
ENSP00000340554.6:p.Leu19922=
|
|
ENST00000359218.10:c.59565C>A
(TTN)
|
ENSP00000352154.5:p.Leu19855=
|
|
ENST00000342175.10:c.59766C>A
(TTN)
|
ENSP00000340554.6:p.Leu19922=
|
|
ENST00000342992.10:c.78681C>A
(TTN)
|
ENSP00000343764.6:p.Leu26227=
|
|
ENST00000359218.9:c.59565C>A
(TTN)
|
ENSP00000352154.5:p.Leu19855=
|
|
ENST00000460472.6:c.59190C>A
(TTN)
|
ENSP00000434586.1:p.Leu19730=
|
|
ENST00000589042.5:c.86385C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu28795=
|
|
ENST00000591111.5:c.81462C>A
(TTN)
|
ENSP00000465570.1:p.Leu27154=
|
|
ENST00000615779.4:c.81462C>A
(TTN)
|
ENSP00000483597.1:p.Leu27154=
|
|
NM_001256850.1:c.81462C>A
(TTN)
|
NP_001243779.1:p.Leu27154=
|
|
NM_001267550.2:c.86385C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Leu28795=
|
|
NM_003319.4:c.59190C>A
(TTN)
|
NP_003310.4:p.Leu19730=
|
|
NM_133378.4:c.78681C>A
(TTN)
|
NP_596869.4:p.Leu26227=
|
|
NM_133432.3:c.59565C>A
(TTN)
|
NP_597676.3:p.Leu19855=
|
|
NM_133437.4:c.59766C>A
(TTN)
|
NP_597681.4:p.Leu19922=
|
|
NR_038271.1:n.447-11553G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+17386G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.85482C>A
(TTN)
|
XP_011510031.1:p.Leu28494=
|
|
XM_011511730.1:c.59376C>A
(TTN)
|
XP_011510032.1:p.Leu19792=
|
|
XM_011511731.1:c.59235C>A
(TTN)
|
XP_011510033.1:p.Leu19745=
|
|
XM_017004819.1:c.85278C>A
(TTN)
|
XP_016860308.1:p.Leu28426=
|
|
XM_017004820.1:c.80676C>A
(TTN)
|
XP_016860309.1:p.Leu26892=
|
|
XM_017004821.1:c.80673C>A
(TTN)
|
XP_016860310.1:p.Leu26891=
|
|
XM_017004822.1:c.77715C>A
(TTN)
|
XP_016860311.1:p.Leu25905=
|
|
XM_017004823.1:c.59331C>A
(TTN)
|
XP_016860312.1:p.Leu19777=
|
|
XM_024453094.1:c.80826C>A
(TTN)
|
XP_024308862.1:p.Leu26942=
|
|
XM_024453095.1:c.80823C>A
(TTN)
|
XP_024308863.1:p.Leu26941=
|
|
XM_024453096.1:c.80256C>A
(TTN)
|
XP_024308864.1:p.Leu26752=
|
|
XM_024453097.1:c.77598C>A
(TTN)
|
XP_024308865.1:p.Leu25866=
|
|
XM_024453098.1:c.77517C>A
(TTN)
|
XP_024308866.1:p.Leu25839=
|
|
XM_024453099.1:c.59280C>A
(TTN)
|
XP_024308867.1:p.Leu19760=
|
|
XM_024453100.1:c.49134C>A
(TTN)
|
XP_024308868.1:p.Leu16378=
|
|