ENST00000342992.11:c.96728A>G
(TTN)
|
ENSP00000343764.6:p.Glu32243Gly
|
|
ENST00000342175.11:c.77813A>G
(TTN)
|
ENSP00000340554.6:p.Glu25938Gly
|
|
ENST00000359218.10:c.77612A>G
(TTN)
|
ENSP00000352154.5:p.Glu25871Gly
|
|
ENST00000342175.10:c.77813A>G
(TTN)
|
ENSP00000340554.6:p.Glu25938Gly
|
|
ENST00000342992.10:c.96728A>G
(TTN)
|
ENSP00000343764.6:p.Glu32243Gly
|
|
ENST00000359218.9:c.77612A>G
(TTN)
|
ENSP00000352154.5:p.Glu25871Gly
|
|
ENST00000460472.6:c.77237A>G
(TTN)
|
ENSP00000434586.1:p.Glu25746Gly
|
|
ENST00000589042.5:c.104432A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu34811Gly
|
|
ENST00000591111.5:c.99509A>G
(TTN)
|
ENSP00000465570.1:p.Glu33170Gly
|
|
ENST00000615779.4:c.99509A>G
(TTN)
|
ENSP00000483597.1:p.Glu33170Gly
|
|
NM_001256850.1:c.99509A>G
(TTN)
|
NP_001243779.1:p.Glu33170Gly
|
|
NM_001267550.2:c.104432A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Glu34811Gly
|
|
NM_003319.4:c.77237A>G
(TTN)
|
NP_003310.4:p.Glu25746Gly
|
|
NM_133378.4:c.96728A>G
(TTN)
|
NP_596869.4:p.Glu32243Gly
|
|
NM_133432.3:c.77612A>G
(TTN)
|
NP_597676.3:p.Glu25871Gly
|
|
NM_133437.4:c.77813A>G
(TTN)
|
NP_597681.4:p.Glu25938Gly
|
|
NR_038271.1:n.446+8547T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3549T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.103529A>G
(TTN)
|
XP_011510031.1:p.Glu34510Gly
|
|
XM_011511730.1:c.77423A>G
(TTN)
|
XP_011510032.1:p.Glu25808Gly
|
|
XM_011511731.1:c.77282A>G
(TTN)
|
XP_011510033.1:p.Glu25761Gly
|
|
XM_017004819.1:c.103325A>G
(TTN)
|
XP_016860308.1:p.Glu34442Gly
|
|
XM_017004820.1:c.98723A>G
(TTN)
|
XP_016860309.1:p.Glu32908Gly
|
|
XM_017004821.1:c.98720A>G
(TTN)
|
XP_016860310.1:p.Glu32907Gly
|
|
XM_017004822.1:c.95762A>G
(TTN)
|
XP_016860311.1:p.Glu31921Gly
|
|
XM_017004823.1:c.77378A>G
(TTN)
|
XP_016860312.1:p.Glu25793Gly
|
|
XM_024453094.1:c.98873A>G
(TTN)
|
XP_024308862.1:p.Glu32958Gly
|
|
XM_024453095.1:c.98870A>G
(TTN)
|
XP_024308863.1:p.Glu32957Gly
|
|
XM_024453096.1:c.98303A>G
(TTN)
|
XP_024308864.1:p.Glu32768Gly
|
|
XM_024453097.1:c.95645A>G
(TTN)
|
XP_024308865.1:p.Glu31882Gly
|
|
XM_024453098.1:c.95564A>G
(TTN)
|
XP_024308866.1:p.Glu31855Gly
|
|
XM_024453099.1:c.77327A>G
(TTN)
|
XP_024308867.1:p.Glu25776Gly
|
|
XM_024453100.1:c.67181A>G
(TTN)
|
XP_024308868.1:p.Glu22394Gly
|
|