ENST00000342992.11:c.50652A>G
(TTN)
|
ENSP00000343764.6:p.Ser16884=
|
|
ENST00000342175.11:c.31737A>G
(TTN)
|
ENSP00000340554.6:p.Ser10579=
|
|
ENST00000359218.10:c.31536A>G
(TTN)
|
ENSP00000352154.5:p.Ser10512=
|
|
ENST00000342175.10:c.31737A>G
(TTN)
|
ENSP00000340554.6:p.Ser10579=
|
|
ENST00000342992.10:c.50652A>G
(TTN)
|
ENSP00000343764.6:p.Ser16884=
|
|
ENST00000359218.9:c.31536A>G
(TTN)
|
ENSP00000352154.5:p.Ser10512=
|
|
ENST00000460472.6:c.31161A>G
(TTN)
|
ENSP00000434586.1:p.Ser10387=
|
|
ENST00000589042.5:c.58356A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ser19452=
|
|
ENST00000591111.5:c.53433A>G
(TTN)
|
ENSP00000465570.1:p.Ser17811=
|
|
ENST00000615779.4:c.53433A>G
(TTN)
|
ENSP00000483597.1:p.Ser17811=
|
|
NM_001256850.1:c.53433A>G
(TTN)
|
NP_001243779.1:p.Ser17811=
|
|
NM_001267550.2:c.58356A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Ser19452=
|
|
NM_003319.4:c.31161A>G
(TTN)
|
NP_003310.4:p.Ser10387=
|
|
NM_133378.4:c.50652A>G
(TTN)
|
NP_596869.4:p.Ser16884=
|
|
NM_133432.3:c.31536A>G
(TTN)
|
NP_597676.3:p.Ser10512=
|
|
NM_133437.4:c.31737A>G
(TTN)
|
NP_597681.4:p.Ser10579=
|
|
NR_038271.1:n.597-3559T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.3364+2723T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.57453A>G
(TTN)
|
XP_011510031.1:p.Ser19151=
|
|
XM_011511730.1:c.31347A>G
(TTN)
|
XP_011510032.1:p.Ser10449=
|
|
XM_011511731.1:c.31206A>G
(TTN)
|
XP_011510033.1:p.Ser10402=
|
|
XM_017004819.1:c.57249A>G
(TTN)
|
XP_016860308.1:p.Ser19083=
|
|
XM_017004820.1:c.52647A>G
(TTN)
|
XP_016860309.1:p.Ser17549=
|
|
XM_017004821.1:c.52644A>G
(TTN)
|
XP_016860310.1:p.Ser17548=
|
|
XM_017004822.1:c.49686A>G
(TTN)
|
XP_016860311.1:p.Ser16562=
|
|
XM_017004823.1:c.31302A>G
(TTN)
|
XP_016860312.1:p.Ser10434=
|
|
XM_024453094.1:c.52797A>G
(TTN)
|
XP_024308862.1:p.Ser17599=
|
|
XM_024453095.1:c.52794A>G
(TTN)
|
XP_024308863.1:p.Ser17598=
|
|
XM_024453096.1:c.52227A>G
(TTN)
|
XP_024308864.1:p.Ser17409=
|
|
XM_024453097.1:c.49569A>G
(TTN)
|
XP_024308865.1:p.Ser16523=
|
|
XM_024453098.1:c.49488A>G
(TTN)
|
XP_024308866.1:p.Ser16496=
|
|
XM_024453099.1:c.31251A>G
(TTN)
|
XP_024308867.1:p.Ser10417=
|
|
XM_024453100.1:c.21105A>G
(TTN)
|
XP_024308868.1:p.Ser7035=
|
|