ENST00000342992.11:c.98685A>C
(TTN)
|
ENSP00000343764.6:p.Gly32895=
|
|
ENST00000342175.11:c.79770A>C
(TTN)
|
ENSP00000340554.6:p.Gly26590=
|
|
ENST00000359218.10:c.79569A>C
(TTN)
|
ENSP00000352154.5:p.Gly26523=
|
|
ENST00000342175.10:c.79770A>C
(TTN)
|
ENSP00000340554.6:p.Gly26590=
|
|
ENST00000342992.10:c.98685A>C
(TTN)
|
ENSP00000343764.6:p.Gly32895=
|
|
ENST00000359218.9:c.79569A>C
(TTN)
|
ENSP00000352154.5:p.Gly26523=
|
|
ENST00000460472.6:c.79194A>C
(TTN)
|
ENSP00000434586.1:p.Gly26398=
|
|
ENST00000589042.5:c.106389A>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gly35463=
|
|
ENST00000591111.5:c.101466A>C
(TTN)
|
ENSP00000465570.1:p.Gly33822=
|
|
ENST00000615779.4:c.101466A>C
(TTN)
|
ENSP00000483597.1:p.Gly33822=
|
|
NM_001256850.1:c.101466A>C
(TTN)
|
NP_001243779.1:p.Gly33822=
|
|
NM_001267550.2:c.106389A>C
(TTN)
MANE Select
|
NP_001254479.2:p.Gly35463=
|
|
NM_003319.4:c.79194A>C
(TTN)
|
NP_003310.4:p.Gly26398=
|
|
NM_133378.4:c.98685A>C
(TTN)
|
NP_596869.4:p.Gly32895=
|
|
NM_133432.3:c.79569A>C
(TTN)
|
NP_597676.3:p.Gly26523=
|
|
NM_133437.4:c.79770A>C
(TTN)
|
NP_597681.4:p.Gly26590=
|
|
NR_038271.1:n.446+6466T>G
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5630T>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.105486A>C
(TTN)
|
XP_011510031.1:p.Gly35162=
|
|
XM_011511730.1:c.79380A>C
(TTN)
|
XP_011510032.1:p.Gly26460=
|
|
XM_011511731.1:c.79239A>C
(TTN)
|
XP_011510033.1:p.Gly26413=
|
|
XM_017004819.1:c.105282A>C
(TTN)
|
XP_016860308.1:p.Gly35094=
|
|
XM_017004820.1:c.100680A>C
(TTN)
|
XP_016860309.1:p.Gly33560=
|
|
XM_017004821.1:c.100677A>C
(TTN)
|
XP_016860310.1:p.Gly33559=
|
|
XM_017004822.1:c.97719A>C
(TTN)
|
XP_016860311.1:p.Gly32573=
|
|
XM_017004823.1:c.79335A>C
(TTN)
|
XP_016860312.1:p.Gly26445=
|
|
XM_024453094.1:c.100830A>C
(TTN)
|
XP_024308862.1:p.Gly33610=
|
|
XM_024453095.1:c.100827A>C
(TTN)
|
XP_024308863.1:p.Gly33609=
|
|
XM_024453096.1:c.100260A>C
(TTN)
|
XP_024308864.1:p.Gly33420=
|
|
XM_024453097.1:c.97602A>C
(TTN)
|
XP_024308865.1:p.Gly32534=
|
|
XM_024453098.1:c.97521A>C
(TTN)
|
XP_024308866.1:p.Gly32507=
|
|
XM_024453099.1:c.79284A>C
(TTN)
|
XP_024308867.1:p.Gly26428=
|
|
XM_024453100.1:c.69138A>C
(TTN)
|
XP_024308868.1:p.Gly23046=
|
|