ENST00000342992.11:c.98273T>G
(TTN)
|
ENSP00000343764.6:p.Leu32758Arg
|
|
ENST00000342175.11:c.79358T>G
(TTN)
|
ENSP00000340554.6:p.Leu26453Arg
|
|
ENST00000359218.10:c.79157T>G
(TTN)
|
ENSP00000352154.5:p.Leu26386Arg
|
|
ENST00000342175.10:c.79358T>G
(TTN)
|
ENSP00000340554.6:p.Leu26453Arg
|
|
ENST00000342992.10:c.98273T>G
(TTN)
|
ENSP00000343764.6:p.Leu32758Arg
|
|
ENST00000359218.9:c.79157T>G
(TTN)
|
ENSP00000352154.5:p.Leu26386Arg
|
|
ENST00000460472.6:c.78782T>G
(TTN)
|
ENSP00000434586.1:p.Leu26261Arg
|
|
ENST00000589042.5:c.105977T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu35326Arg
|
|
ENST00000591111.5:c.101054T>G
(TTN)
|
ENSP00000465570.1:p.Leu33685Arg
|
|
ENST00000615779.4:c.101054T>G
(TTN)
|
ENSP00000483597.1:p.Leu33685Arg
|
|
NM_001256850.1:c.101054T>G
(TTN)
|
NP_001243779.1:p.Leu33685Arg
|
|
NM_001267550.2:c.105977T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Leu35326Arg
|
|
NM_003319.4:c.78782T>G
(TTN)
|
NP_003310.4:p.Leu26261Arg
|
|
NM_133378.4:c.98273T>G
(TTN)
|
NP_596869.4:p.Leu32758Arg
|
|
NM_133432.3:c.79157T>G
(TTN)
|
NP_597676.3:p.Leu26386Arg
|
|
NM_133437.4:c.79358T>G
(TTN)
|
NP_597681.4:p.Leu26453Arg
|
|
NR_038271.1:n.446+7002A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5094A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.105074T>G
(TTN)
|
XP_011510031.1:p.Leu35025Arg
|
|
XM_011511730.1:c.78968T>G
(TTN)
|
XP_011510032.1:p.Leu26323Arg
|
|
XM_011511731.1:c.78827T>G
(TTN)
|
XP_011510033.1:p.Leu26276Arg
|
|
XM_017004819.1:c.104870T>G
(TTN)
|
XP_016860308.1:p.Leu34957Arg
|
|
XM_017004820.1:c.100268T>G
(TTN)
|
XP_016860309.1:p.Leu33423Arg
|
|
XM_017004821.1:c.100265T>G
(TTN)
|
XP_016860310.1:p.Leu33422Arg
|
|
XM_017004822.1:c.97307T>G
(TTN)
|
XP_016860311.1:p.Leu32436Arg
|
|
XM_017004823.1:c.78923T>G
(TTN)
|
XP_016860312.1:p.Leu26308Arg
|
|
XM_024453094.1:c.100418T>G
(TTN)
|
XP_024308862.1:p.Leu33473Arg
|
|
XM_024453095.1:c.100415T>G
(TTN)
|
XP_024308863.1:p.Leu33472Arg
|
|
XM_024453096.1:c.99848T>G
(TTN)
|
XP_024308864.1:p.Leu33283Arg
|
|
XM_024453097.1:c.97190T>G
(TTN)
|
XP_024308865.1:p.Leu32397Arg
|
|
XM_024453098.1:c.97109T>G
(TTN)
|
XP_024308866.1:p.Leu32370Arg
|
|
XM_024453099.1:c.78872T>G
(TTN)
|
XP_024308867.1:p.Leu26291Arg
|
|
XM_024453100.1:c.68726T>G
(TTN)
|
XP_024308868.1:p.Leu22909Arg
|
|