ENST00000342992.11:c.86956G>A
(TTN)
|
ENSP00000343764.6:p.Gly28986Ser
|
|
ENST00000342175.11:c.68041G>A
(TTN)
|
ENSP00000340554.6:p.Gly22681Ser
|
|
ENST00000359218.10:c.67840G>A
(TTN)
|
ENSP00000352154.5:p.Gly22614Ser
|
|
ENST00000342175.10:c.68041G>A
(TTN)
|
ENSP00000340554.6:p.Gly22681Ser
|
|
ENST00000342992.10:c.86956G>A
(TTN)
|
ENSP00000343764.6:p.Gly28986Ser
|
|
ENST00000359218.9:c.67840G>A
(TTN)
|
ENSP00000352154.5:p.Gly22614Ser
|
|
ENST00000460472.6:c.67465G>A
(TTN)
|
ENSP00000434586.1:p.Gly22489Ser
|
|
ENST00000589042.5:c.94660G>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gly31554Ser
|
|
ENST00000591111.5:c.89737G>A
(TTN)
|
ENSP00000465570.1:p.Gly29913Ser
|
|
ENST00000615779.4:c.89737G>A
(TTN)
|
ENSP00000483597.1:p.Gly29913Ser
|
|
NM_001256850.1:c.89737G>A
(TTN)
|
NP_001243779.1:p.Gly29913Ser
|
|
NM_001267550.2:c.94660G>A
(TTN)
MANE Select
|
NP_001254479.2:p.Gly31554Ser
|
|
NM_003319.4:c.67465G>A
(TTN)
|
NP_003310.4:p.Gly22489Ser
|
|
NM_133378.4:c.86956G>A
(TTN)
|
NP_596869.4:p.Gly28986Ser
|
|
NM_133432.3:c.67840G>A
(TTN)
|
NP_597676.3:p.Gly22614Ser
|
|
NM_133437.4:c.68041G>A
(TTN)
|
NP_597681.4:p.Gly22681Ser
|
|
NR_038271.1:n.446+23132C>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+4407C>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.93757G>A
(TTN)
|
XP_011510031.1:p.Gly31253Ser
|
|
XM_011511730.1:c.67651G>A
(TTN)
|
XP_011510032.1:p.Gly22551Ser
|
|
XM_011511731.1:c.67510G>A
(TTN)
|
XP_011510033.1:p.Gly22504Ser
|
|
XM_017004819.1:c.93553G>A
(TTN)
|
XP_016860308.1:p.Gly31185Ser
|
|
XM_017004820.1:c.88951G>A
(TTN)
|
XP_016860309.1:p.Gly29651Ser
|
|
XM_017004821.1:c.88948G>A
(TTN)
|
XP_016860310.1:p.Gly29650Ser
|
|
XM_017004822.1:c.85990G>A
(TTN)
|
XP_016860311.1:p.Gly28664Ser
|
|
XM_017004823.1:c.67606G>A
(TTN)
|
XP_016860312.1:p.Gly22536Ser
|
|
XM_024453094.1:c.89101G>A
(TTN)
|
XP_024308862.1:p.Gly29701Ser
|
|
XM_024453095.1:c.89098G>A
(TTN)
|
XP_024308863.1:p.Gly29700Ser
|
|
XM_024453096.1:c.88531G>A
(TTN)
|
XP_024308864.1:p.Gly29511Ser
|
|
XM_024453097.1:c.85873G>A
(TTN)
|
XP_024308865.1:p.Gly28625Ser
|
|
XM_024453098.1:c.85792G>A
(TTN)
|
XP_024308866.1:p.Gly28598Ser
|
|
XM_024453099.1:c.67555G>A
(TTN)
|
XP_024308867.1:p.Gly22519Ser
|
|
XM_024453100.1:c.57409G>A
(TTN)
|
XP_024308868.1:p.Gly19137Ser
|
|