ENST00000342992.11:c.98718G>A
(TTN)
|
ENSP00000343764.6:p.Gly32906=
|
|
ENST00000342175.11:c.79803G>A
(TTN)
|
ENSP00000340554.6:p.Gly26601=
|
|
ENST00000359218.10:c.79602G>A
(TTN)
|
ENSP00000352154.5:p.Gly26534=
|
|
ENST00000342175.10:c.79803G>A
(TTN)
|
ENSP00000340554.6:p.Gly26601=
|
|
ENST00000342992.10:c.98718G>A
(TTN)
|
ENSP00000343764.6:p.Gly32906=
|
|
ENST00000359218.9:c.79602G>A
(TTN)
|
ENSP00000352154.5:p.Gly26534=
|
|
ENST00000460472.6:c.79227G>A
(TTN)
|
ENSP00000434586.1:p.Gly26409=
|
|
ENST00000589042.5:c.106422G>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gly35474=
|
|
ENST00000591111.5:c.101499G>A
(TTN)
|
ENSP00000465570.1:p.Gly33833=
|
|
ENST00000615779.4:c.101499G>A
(TTN)
|
ENSP00000483597.1:p.Gly33833=
|
|
NM_001256850.1:c.101499G>A
(TTN)
|
NP_001243779.1:p.Gly33833=
|
|
NM_001267550.2:c.106422G>A
(TTN)
MANE Select
|
NP_001254479.2:p.Gly35474=
|
|
NM_003319.4:c.79227G>A
(TTN)
|
NP_003310.4:p.Gly26409=
|
|
NM_133378.4:c.98718G>A
(TTN)
|
NP_596869.4:p.Gly32906=
|
|
NM_133432.3:c.79602G>A
(TTN)
|
NP_597676.3:p.Gly26534=
|
|
NM_133437.4:c.79803G>A
(TTN)
|
NP_597681.4:p.Gly26601=
|
|
NR_038271.1:n.446+6433C>T
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5663C>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.105519G>A
(TTN)
|
XP_011510031.1:p.Gly35173=
|
|
XM_011511730.1:c.79413G>A
(TTN)
|
XP_011510032.1:p.Gly26471=
|
|
XM_011511731.1:c.79272G>A
(TTN)
|
XP_011510033.1:p.Gly26424=
|
|
XM_017004819.1:c.105315G>A
(TTN)
|
XP_016860308.1:p.Gly35105=
|
|
XM_017004820.1:c.100713G>A
(TTN)
|
XP_016860309.1:p.Gly33571=
|
|
XM_017004821.1:c.100710G>A
(TTN)
|
XP_016860310.1:p.Gly33570=
|
|
XM_017004822.1:c.97752G>A
(TTN)
|
XP_016860311.1:p.Gly32584=
|
|
XM_017004823.1:c.79368G>A
(TTN)
|
XP_016860312.1:p.Gly26456=
|
|
XM_024453094.1:c.100863G>A
(TTN)
|
XP_024308862.1:p.Gly33621=
|
|
XM_024453095.1:c.100860G>A
(TTN)
|
XP_024308863.1:p.Gly33620=
|
|
XM_024453096.1:c.100293G>A
(TTN)
|
XP_024308864.1:p.Gly33431=
|
|
XM_024453097.1:c.97635G>A
(TTN)
|
XP_024308865.1:p.Gly32545=
|
|
XM_024453098.1:c.97554G>A
(TTN)
|
XP_024308866.1:p.Gly32518=
|
|
XM_024453099.1:c.79317G>A
(TTN)
|
XP_024308867.1:p.Gly26439=
|
|
XM_024453100.1:c.69171G>A
(TTN)
|
XP_024308868.1:p.Gly23057=
|
|