ENST00000342992.11:c.96747A>G
(TTN)
|
ENSP00000343764.6:p.Glu32249=
|
|
ENST00000342175.11:c.77832A>G
(TTN)
|
ENSP00000340554.6:p.Glu25944=
|
|
ENST00000359218.10:c.77631A>G
(TTN)
|
ENSP00000352154.5:p.Glu25877=
|
|
ENST00000342175.10:c.77832A>G
(TTN)
|
ENSP00000340554.6:p.Glu25944=
|
|
ENST00000342992.10:c.96747A>G
(TTN)
|
ENSP00000343764.6:p.Glu32249=
|
|
ENST00000359218.9:c.77631A>G
(TTN)
|
ENSP00000352154.5:p.Glu25877=
|
|
ENST00000460472.6:c.77256A>G
(TTN)
|
ENSP00000434586.1:p.Glu25752=
|
|
ENST00000589042.5:c.104451A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu34817=
|
|
ENST00000591111.5:c.99528A>G
(TTN)
|
ENSP00000465570.1:p.Glu33176=
|
|
ENST00000615779.4:c.99528A>G
(TTN)
|
ENSP00000483597.1:p.Glu33176=
|
|
NM_001256850.1:c.99528A>G
(TTN)
|
NP_001243779.1:p.Glu33176=
|
|
NM_001267550.2:c.104451A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Glu34817=
|
|
NM_003319.4:c.77256A>G
(TTN)
|
NP_003310.4:p.Glu25752=
|
|
NM_133378.4:c.96747A>G
(TTN)
|
NP_596869.4:p.Glu32249=
|
|
NM_133432.3:c.77631A>G
(TTN)
|
NP_597676.3:p.Glu25877=
|
|
NM_133437.4:c.77832A>G
(TTN)
|
NP_597681.4:p.Glu25944=
|
|
NR_038271.1:n.446+8528T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3568T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.103548A>G
(TTN)
|
XP_011510031.1:p.Glu34516=
|
|
XM_011511730.1:c.77442A>G
(TTN)
|
XP_011510032.1:p.Glu25814=
|
|
XM_011511731.1:c.77301A>G
(TTN)
|
XP_011510033.1:p.Glu25767=
|
|
XM_017004819.1:c.103344A>G
(TTN)
|
XP_016860308.1:p.Glu34448=
|
|
XM_017004820.1:c.98742A>G
(TTN)
|
XP_016860309.1:p.Glu32914=
|
|
XM_017004821.1:c.98739A>G
(TTN)
|
XP_016860310.1:p.Glu32913=
|
|
XM_017004822.1:c.95781A>G
(TTN)
|
XP_016860311.1:p.Glu31927=
|
|
XM_017004823.1:c.77397A>G
(TTN)
|
XP_016860312.1:p.Glu25799=
|
|
XM_024453094.1:c.98892A>G
(TTN)
|
XP_024308862.1:p.Glu32964=
|
|
XM_024453095.1:c.98889A>G
(TTN)
|
XP_024308863.1:p.Glu32963=
|
|
XM_024453096.1:c.98322A>G
(TTN)
|
XP_024308864.1:p.Glu32774=
|
|
XM_024453097.1:c.95664A>G
(TTN)
|
XP_024308865.1:p.Glu31888=
|
|
XM_024453098.1:c.95583A>G
(TTN)
|
XP_024308866.1:p.Glu31861=
|
|
XM_024453099.1:c.77346A>G
(TTN)
|
XP_024308867.1:p.Glu25782=
|
|
XM_024453100.1:c.67200A>G
(TTN)
|
XP_024308868.1:p.Glu22400=
|
|