ENST00000342992.11:c.82634A>G
(TTN)
|
ENSP00000343764.6:p.Asp27545Gly
|
|
ENST00000342175.11:c.63719A>G
(TTN)
|
ENSP00000340554.6:p.Asp21240Gly
|
|
ENST00000359218.10:c.63518A>G
(TTN)
|
ENSP00000352154.5:p.Asp21173Gly
|
|
ENST00000342175.10:c.63719A>G
(TTN)
|
ENSP00000340554.6:p.Asp21240Gly
|
|
ENST00000342992.10:c.82634A>G
(TTN)
|
ENSP00000343764.6:p.Asp27545Gly
|
|
ENST00000359218.9:c.63518A>G
(TTN)
|
ENSP00000352154.5:p.Asp21173Gly
|
|
ENST00000460472.6:c.63143A>G
(TTN)
|
ENSP00000434586.1:p.Asp21048Gly
|
|
ENST00000589042.5:c.90338A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp30113Gly
|
|
ENST00000591111.5:c.85415A>G
(TTN)
|
ENSP00000465570.1:p.Asp28472Gly
|
|
ENST00000615779.4:c.85415A>G
(TTN)
|
ENSP00000483597.1:p.Asp28472Gly
|
|
NM_001256850.1:c.85415A>G
(TTN)
|
NP_001243779.1:p.Asp28472Gly
|
|
NM_001267550.2:c.90338A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Asp30113Gly
|
|
NM_003319.4:c.63143A>G
(TTN)
|
NP_003310.4:p.Asp21048Gly
|
|
NM_133378.4:c.82634A>G
(TTN)
|
NP_596869.4:p.Asp27545Gly
|
|
NM_133432.3:c.63518A>G
(TTN)
|
NP_597676.3:p.Asp21173Gly
|
|
NM_133437.4:c.63719A>G
(TTN)
|
NP_597681.4:p.Asp21240Gly
|
|
NR_038271.1:n.447-18738T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+10201T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.89435A>G
(TTN)
|
XP_011510031.1:p.Asp29812Gly
|
|
XM_011511730.1:c.63329A>G
(TTN)
|
XP_011510032.1:p.Asp21110Gly
|
|
XM_011511731.1:c.63188A>G
(TTN)
|
XP_011510033.1:p.Asp21063Gly
|
|
XM_017004819.1:c.89231A>G
(TTN)
|
XP_016860308.1:p.Asp29744Gly
|
|
XM_017004820.1:c.84629A>G
(TTN)
|
XP_016860309.1:p.Asp28210Gly
|
|
XM_017004821.1:c.84626A>G
(TTN)
|
XP_016860310.1:p.Asp28209Gly
|
|
XM_017004822.1:c.81668A>G
(TTN)
|
XP_016860311.1:p.Asp27223Gly
|
|
XM_017004823.1:c.63284A>G
(TTN)
|
XP_016860312.1:p.Asp21095Gly
|
|
XM_024453094.1:c.84779A>G
(TTN)
|
XP_024308862.1:p.Asp28260Gly
|
|
XM_024453095.1:c.84776A>G
(TTN)
|
XP_024308863.1:p.Asp28259Gly
|
|
XM_024453096.1:c.84209A>G
(TTN)
|
XP_024308864.1:p.Asp28070Gly
|
|
XM_024453097.1:c.81551A>G
(TTN)
|
XP_024308865.1:p.Asp27184Gly
|
|
XM_024453098.1:c.81470A>G
(TTN)
|
XP_024308866.1:p.Asp27157Gly
|
|
XM_024453099.1:c.63233A>G
(TTN)
|
XP_024308867.1:p.Asp21078Gly
|
|
XM_024453100.1:c.53087A>G
(TTN)
|
XP_024308868.1:p.Asp17696Gly
|
|