ENST00000342992.11:c.83517A>G
(TTN)
|
ENSP00000343764.6:p.Leu27839=
|
|
ENST00000342175.11:c.64602A>G
(TTN)
|
ENSP00000340554.6:p.Leu21534=
|
|
ENST00000359218.10:c.64401A>G
(TTN)
|
ENSP00000352154.5:p.Leu21467=
|
|
ENST00000342175.10:c.64602A>G
(TTN)
|
ENSP00000340554.6:p.Leu21534=
|
|
ENST00000342992.10:c.83517A>G
(TTN)
|
ENSP00000343764.6:p.Leu27839=
|
|
ENST00000359218.9:c.64401A>G
(TTN)
|
ENSP00000352154.5:p.Leu21467=
|
|
ENST00000460472.6:c.64026A>G
(TTN)
|
ENSP00000434586.1:p.Leu21342=
|
|
ENST00000589042.5:c.91221A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu30407=
|
|
ENST00000591111.5:c.86298A>G
(TTN)
|
ENSP00000465570.1:p.Leu28766=
|
|
ENST00000615779.4:c.86298A>G
(TTN)
|
ENSP00000483597.1:p.Leu28766=
|
|
NM_001256850.1:c.86298A>G
(TTN)
|
NP_001243779.1:p.Leu28766=
|
|
NM_001267550.2:c.91221A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Leu30407=
|
|
NM_003319.4:c.64026A>G
(TTN)
|
NP_003310.4:p.Leu21342=
|
|
NM_133378.4:c.83517A>G
(TTN)
|
NP_596869.4:p.Leu27839=
|
|
NM_133432.3:c.64401A>G
(TTN)
|
NP_597676.3:p.Leu21467=
|
|
NM_133437.4:c.64602A>G
(TTN)
|
NP_597681.4:p.Leu21534=
|
|
NR_038271.1:n.447-19621T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+9318T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.90318A>G
(TTN)
|
XP_011510031.1:p.Leu30106=
|
|
XM_011511730.1:c.64212A>G
(TTN)
|
XP_011510032.1:p.Leu21404=
|
|
XM_011511731.1:c.64071A>G
(TTN)
|
XP_011510033.1:p.Leu21357=
|
|
XM_017004819.1:c.90114A>G
(TTN)
|
XP_016860308.1:p.Leu30038=
|
|
XM_017004820.1:c.85512A>G
(TTN)
|
XP_016860309.1:p.Leu28504=
|
|
XM_017004821.1:c.85509A>G
(TTN)
|
XP_016860310.1:p.Leu28503=
|
|
XM_017004822.1:c.82551A>G
(TTN)
|
XP_016860311.1:p.Leu27517=
|
|
XM_017004823.1:c.64167A>G
(TTN)
|
XP_016860312.1:p.Leu21389=
|
|
XM_024453094.1:c.85662A>G
(TTN)
|
XP_024308862.1:p.Leu28554=
|
|
XM_024453095.1:c.85659A>G
(TTN)
|
XP_024308863.1:p.Leu28553=
|
|
XM_024453096.1:c.85092A>G
(TTN)
|
XP_024308864.1:p.Leu28364=
|
|
XM_024453097.1:c.82434A>G
(TTN)
|
XP_024308865.1:p.Leu27478=
|
|
XM_024453098.1:c.82353A>G
(TTN)
|
XP_024308866.1:p.Leu27451=
|
|
XM_024453099.1:c.64116A>G
(TTN)
|
XP_024308867.1:p.Leu21372=
|
|
XM_024453100.1:c.53970A>G
(TTN)
|
XP_024308868.1:p.Leu17990=
|
|