ENST00000342992.11:c.91798G>T
(TTN)
|
ENSP00000343764.6:p.Glu30600Ter
|
|
ENST00000342175.11:c.72883G>T
(TTN)
|
ENSP00000340554.6:p.Glu24295Ter
|
|
ENST00000359218.10:c.72682G>T
(TTN)
|
ENSP00000352154.5:p.Glu24228Ter
|
|
ENST00000342175.10:c.72883G>T
(TTN)
|
ENSP00000340554.6:p.Glu24295Ter
|
|
ENST00000342992.10:c.91798G>T
(TTN)
|
ENSP00000343764.6:p.Glu30600Ter
|
|
ENST00000359218.9:c.72682G>T
(TTN)
|
ENSP00000352154.5:p.Glu24228Ter
|
|
ENST00000460472.6:c.72307G>T
(TTN)
|
ENSP00000434586.1:p.Glu24103Ter
|
|
ENST00000589042.5:c.99502G>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu33168Ter
|
|
ENST00000591111.5:c.94579G>T
(TTN)
|
ENSP00000465570.1:p.Glu31527Ter
|
|
ENST00000615779.4:c.94579G>T
(TTN)
|
ENSP00000483597.1:p.Glu31527Ter
|
|
NM_001256850.1:c.94579G>T
(TTN)
|
NP_001243779.1:p.Glu31527Ter
|
|
NM_001267550.2:c.99502G>T
(TTN)
MANE Select
|
NP_001254479.2:p.Glu33168Ter
|
|
NM_003319.4:c.72307G>T
(TTN)
|
NP_003310.4:p.Glu24103Ter
|
|
NM_133378.4:c.91798G>T
(TTN)
|
NP_596869.4:p.Glu30600Ter
|
|
NM_133432.3:c.72682G>T
(TTN)
|
NP_597676.3:p.Glu24228Ter
|
|
NM_133437.4:c.72883G>T
(TTN)
|
NP_597681.4:p.Glu24295Ter
|
|
NR_038271.1:n.446+14069C>A
(TTN-AS1)
|
|
|
NR_038272.1:n.647+14C>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.98599G>T
(TTN)
|
XP_011510031.1:p.Glu32867Ter
|
|
XM_011511730.1:c.72493G>T
(TTN)
|
XP_011510032.1:p.Glu24165Ter
|
|
XM_011511731.1:c.72352G>T
(TTN)
|
XP_011510033.1:p.Glu24118Ter
|
|
XM_017004819.1:c.98395G>T
(TTN)
|
XP_016860308.1:p.Glu32799Ter
|
|
XM_017004820.1:c.93793G>T
(TTN)
|
XP_016860309.1:p.Glu31265Ter
|
|
XM_017004821.1:c.93790G>T
(TTN)
|
XP_016860310.1:p.Glu31264Ter
|
|
XM_017004822.1:c.90832G>T
(TTN)
|
XP_016860311.1:p.Glu30278Ter
|
|
XM_017004823.1:c.72448G>T
(TTN)
|
XP_016860312.1:p.Glu24150Ter
|
|
XM_024453094.1:c.93943G>T
(TTN)
|
XP_024308862.1:p.Glu31315Ter
|
|
XM_024453095.1:c.93940G>T
(TTN)
|
XP_024308863.1:p.Glu31314Ter
|
|
XM_024453096.1:c.93373G>T
(TTN)
|
XP_024308864.1:p.Glu31125Ter
|
|
XM_024453097.1:c.90715G>T
(TTN)
|
XP_024308865.1:p.Glu30239Ter
|
|
XM_024453098.1:c.90634G>T
(TTN)
|
XP_024308866.1:p.Glu30212Ter
|
|
XM_024453099.1:c.72397G>T
(TTN)
|
XP_024308867.1:p.Glu24133Ter
|
|
XM_024453100.1:c.62251G>T
(TTN)
|
XP_024308868.1:p.Glu20751Ter
|
|