ENST00000342992.11:c.96743A>G
(TTN)
|
ENSP00000343764.6:p.Glu32248Gly
|
|
ENST00000342175.11:c.77828A>G
(TTN)
|
ENSP00000340554.6:p.Glu25943Gly
|
|
ENST00000359218.10:c.77627A>G
(TTN)
|
ENSP00000352154.5:p.Glu25876Gly
|
|
ENST00000342175.10:c.77828A>G
(TTN)
|
ENSP00000340554.6:p.Glu25943Gly
|
|
ENST00000342992.10:c.96743A>G
(TTN)
|
ENSP00000343764.6:p.Glu32248Gly
|
|
ENST00000359218.9:c.77627A>G
(TTN)
|
ENSP00000352154.5:p.Glu25876Gly
|
|
ENST00000460472.6:c.77252A>G
(TTN)
|
ENSP00000434586.1:p.Glu25751Gly
|
|
ENST00000589042.5:c.104447A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu34816Gly
|
|
ENST00000591111.5:c.99524A>G
(TTN)
|
ENSP00000465570.1:p.Glu33175Gly
|
|
ENST00000615779.4:c.99524A>G
(TTN)
|
ENSP00000483597.1:p.Glu33175Gly
|
|
NM_001256850.1:c.99524A>G
(TTN)
|
NP_001243779.1:p.Glu33175Gly
|
|
NM_001267550.2:c.104447A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Glu34816Gly
|
|
NM_003319.4:c.77252A>G
(TTN)
|
NP_003310.4:p.Glu25751Gly
|
|
NM_133378.4:c.96743A>G
(TTN)
|
NP_596869.4:p.Glu32248Gly
|
|
NM_133432.3:c.77627A>G
(TTN)
|
NP_597676.3:p.Glu25876Gly
|
|
NM_133437.4:c.77828A>G
(TTN)
|
NP_597681.4:p.Glu25943Gly
|
|
NR_038271.1:n.446+8532T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3564T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.103544A>G
(TTN)
|
XP_011510031.1:p.Glu34515Gly
|
|
XM_011511730.1:c.77438A>G
(TTN)
|
XP_011510032.1:p.Glu25813Gly
|
|
XM_011511731.1:c.77297A>G
(TTN)
|
XP_011510033.1:p.Glu25766Gly
|
|
XM_017004819.1:c.103340A>G
(TTN)
|
XP_016860308.1:p.Glu34447Gly
|
|
XM_017004820.1:c.98738A>G
(TTN)
|
XP_016860309.1:p.Glu32913Gly
|
|
XM_017004821.1:c.98735A>G
(TTN)
|
XP_016860310.1:p.Glu32912Gly
|
|
XM_017004822.1:c.95777A>G
(TTN)
|
XP_016860311.1:p.Glu31926Gly
|
|
XM_017004823.1:c.77393A>G
(TTN)
|
XP_016860312.1:p.Glu25798Gly
|
|
XM_024453094.1:c.98888A>G
(TTN)
|
XP_024308862.1:p.Glu32963Gly
|
|
XM_024453095.1:c.98885A>G
(TTN)
|
XP_024308863.1:p.Glu32962Gly
|
|
XM_024453096.1:c.98318A>G
(TTN)
|
XP_024308864.1:p.Glu32773Gly
|
|
XM_024453097.1:c.95660A>G
(TTN)
|
XP_024308865.1:p.Glu31887Gly
|
|
XM_024453098.1:c.95579A>G
(TTN)
|
XP_024308866.1:p.Glu31860Gly
|
|
XM_024453099.1:c.77342A>G
(TTN)
|
XP_024308867.1:p.Glu25781Gly
|
|
XM_024453100.1:c.67196A>G
(TTN)
|
XP_024308868.1:p.Glu22399Gly
|
|