ENST00000342992.11:c.86951G>T
(TTN)
|
ENSP00000343764.6:p.Gly28984Val
|
|
ENST00000342175.11:c.68036G>T
(TTN)
|
ENSP00000340554.6:p.Gly22679Val
|
|
ENST00000359218.10:c.67835G>T
(TTN)
|
ENSP00000352154.5:p.Gly22612Val
|
|
ENST00000342175.10:c.68036G>T
(TTN)
|
ENSP00000340554.6:p.Gly22679Val
|
|
ENST00000342992.10:c.86951G>T
(TTN)
|
ENSP00000343764.6:p.Gly28984Val
|
|
ENST00000359218.9:c.67835G>T
(TTN)
|
ENSP00000352154.5:p.Gly22612Val
|
|
ENST00000460472.6:c.67460G>T
(TTN)
|
ENSP00000434586.1:p.Gly22487Val
|
|
ENST00000589042.5:c.94655G>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gly31552Val
|
|
ENST00000591111.5:c.89732G>T
(TTN)
|
ENSP00000465570.1:p.Gly29911Val
|
|
ENST00000615779.4:c.89732G>T
(TTN)
|
ENSP00000483597.1:p.Gly29911Val
|
|
NM_001256850.1:c.89732G>T
(TTN)
|
NP_001243779.1:p.Gly29911Val
|
|
NM_001267550.2:c.94655G>T
(TTN)
MANE Select
|
NP_001254479.2:p.Gly31552Val
|
|
NM_003319.4:c.67460G>T
(TTN)
|
NP_003310.4:p.Gly22487Val
|
|
NM_133378.4:c.86951G>T
(TTN)
|
NP_596869.4:p.Gly28984Val
|
|
NM_133432.3:c.67835G>T
(TTN)
|
NP_597676.3:p.Gly22612Val
|
|
NM_133437.4:c.68036G>T
(TTN)
|
NP_597681.4:p.Gly22679Val
|
|
NR_038271.1:n.446+23137C>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+4412C>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.93752G>T
(TTN)
|
XP_011510031.1:p.Gly31251Val
|
|
XM_011511730.1:c.67646G>T
(TTN)
|
XP_011510032.1:p.Gly22549Val
|
|
XM_011511731.1:c.67505G>T
(TTN)
|
XP_011510033.1:p.Gly22502Val
|
|
XM_017004819.1:c.93548G>T
(TTN)
|
XP_016860308.1:p.Gly31183Val
|
|
XM_017004820.1:c.88946G>T
(TTN)
|
XP_016860309.1:p.Gly29649Val
|
|
XM_017004821.1:c.88943G>T
(TTN)
|
XP_016860310.1:p.Gly29648Val
|
|
XM_017004822.1:c.85985G>T
(TTN)
|
XP_016860311.1:p.Gly28662Val
|
|
XM_017004823.1:c.67601G>T
(TTN)
|
XP_016860312.1:p.Gly22534Val
|
|
XM_024453094.1:c.89096G>T
(TTN)
|
XP_024308862.1:p.Gly29699Val
|
|
XM_024453095.1:c.89093G>T
(TTN)
|
XP_024308863.1:p.Gly29698Val
|
|
XM_024453096.1:c.88526G>T
(TTN)
|
XP_024308864.1:p.Gly29509Val
|
|
XM_024453097.1:c.85868G>T
(TTN)
|
XP_024308865.1:p.Gly28623Val
|
|
XM_024453098.1:c.85787G>T
(TTN)
|
XP_024308866.1:p.Gly28596Val
|
|
XM_024453099.1:c.67550G>T
(TTN)
|
XP_024308867.1:p.Gly22517Val
|
|
XM_024453100.1:c.57404G>T
(TTN)
|
XP_024308868.1:p.Gly19135Val
|
|