ENST00000342992.11:c.98679A>G
(TTN)
|
ENSP00000343764.6:p.Thr32893=
|
|
ENST00000342175.11:c.79764A>G
(TTN)
|
ENSP00000340554.6:p.Thr26588=
|
|
ENST00000359218.10:c.79563A>G
(TTN)
|
ENSP00000352154.5:p.Thr26521=
|
|
ENST00000342175.10:c.79764A>G
(TTN)
|
ENSP00000340554.6:p.Thr26588=
|
|
ENST00000342992.10:c.98679A>G
(TTN)
|
ENSP00000343764.6:p.Thr32893=
|
|
ENST00000359218.9:c.79563A>G
(TTN)
|
ENSP00000352154.5:p.Thr26521=
|
|
ENST00000460472.6:c.79188A>G
(TTN)
|
ENSP00000434586.1:p.Thr26396=
|
|
ENST00000589042.5:c.106383A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr35461=
|
|
ENST00000591111.5:c.101460A>G
(TTN)
|
ENSP00000465570.1:p.Thr33820=
|
|
ENST00000615779.4:c.101460A>G
(TTN)
|
ENSP00000483597.1:p.Thr33820=
|
|
NM_001256850.1:c.101460A>G
(TTN)
|
NP_001243779.1:p.Thr33820=
|
|
NM_001267550.2:c.106383A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Thr35461=
|
|
NM_003319.4:c.79188A>G
(TTN)
|
NP_003310.4:p.Thr26396=
|
|
NM_133378.4:c.98679A>G
(TTN)
|
NP_596869.4:p.Thr32893=
|
|
NM_133432.3:c.79563A>G
(TTN)
|
NP_597676.3:p.Thr26521=
|
|
NM_133437.4:c.79764A>G
(TTN)
|
NP_597681.4:p.Thr26588=
|
|
NR_038271.1:n.446+6472T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5624T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.105480A>G
(TTN)
|
XP_011510031.1:p.Thr35160=
|
|
XM_011511730.1:c.79374A>G
(TTN)
|
XP_011510032.1:p.Thr26458=
|
|
XM_011511731.1:c.79233A>G
(TTN)
|
XP_011510033.1:p.Thr26411=
|
|
XM_017004819.1:c.105276A>G
(TTN)
|
XP_016860308.1:p.Thr35092=
|
|
XM_017004820.1:c.100674A>G
(TTN)
|
XP_016860309.1:p.Thr33558=
|
|
XM_017004821.1:c.100671A>G
(TTN)
|
XP_016860310.1:p.Thr33557=
|
|
XM_017004822.1:c.97713A>G
(TTN)
|
XP_016860311.1:p.Thr32571=
|
|
XM_017004823.1:c.79329A>G
(TTN)
|
XP_016860312.1:p.Thr26443=
|
|
XM_024453094.1:c.100824A>G
(TTN)
|
XP_024308862.1:p.Thr33608=
|
|
XM_024453095.1:c.100821A>G
(TTN)
|
XP_024308863.1:p.Thr33607=
|
|
XM_024453096.1:c.100254A>G
(TTN)
|
XP_024308864.1:p.Thr33418=
|
|
XM_024453097.1:c.97596A>G
(TTN)
|
XP_024308865.1:p.Thr32532=
|
|
XM_024453098.1:c.97515A>G
(TTN)
|
XP_024308866.1:p.Thr32505=
|
|
XM_024453099.1:c.79278A>G
(TTN)
|
XP_024308867.1:p.Thr26426=
|
|
XM_024453100.1:c.69132A>G
(TTN)
|
XP_024308868.1:p.Thr23044=
|
|