ENST00000342992.11:c.98361A>G
(TTN)
|
ENSP00000343764.6:p.Gly32787=
|
|
ENST00000342175.11:c.79446A>G
(TTN)
|
ENSP00000340554.6:p.Gly26482=
|
|
ENST00000359218.10:c.79245A>G
(TTN)
|
ENSP00000352154.5:p.Gly26415=
|
|
ENST00000342175.10:c.79446A>G
(TTN)
|
ENSP00000340554.6:p.Gly26482=
|
|
ENST00000342992.10:c.98361A>G
(TTN)
|
ENSP00000343764.6:p.Gly32787=
|
|
ENST00000359218.9:c.79245A>G
(TTN)
|
ENSP00000352154.5:p.Gly26415=
|
|
ENST00000460472.6:c.78870A>G
(TTN)
|
ENSP00000434586.1:p.Gly26290=
|
|
ENST00000589042.5:c.106065A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gly35355=
|
|
ENST00000591111.5:c.101142A>G
(TTN)
|
ENSP00000465570.1:p.Gly33714=
|
|
ENST00000615779.4:c.101142A>G
(TTN)
|
ENSP00000483597.1:p.Gly33714=
|
|
NM_001256850.1:c.101142A>G
(TTN)
|
NP_001243779.1:p.Gly33714=
|
|
NM_001267550.2:c.106065A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Gly35355=
|
|
NM_003319.4:c.78870A>G
(TTN)
|
NP_003310.4:p.Gly26290=
|
|
NM_133378.4:c.98361A>G
(TTN)
|
NP_596869.4:p.Gly32787=
|
|
NM_133432.3:c.79245A>G
(TTN)
|
NP_597676.3:p.Gly26415=
|
|
NM_133437.4:c.79446A>G
(TTN)
|
NP_597681.4:p.Gly26482=
|
|
NR_038271.1:n.446+6914T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5182T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.105162A>G
(TTN)
|
XP_011510031.1:p.Gly35054=
|
|
XM_011511730.1:c.79056A>G
(TTN)
|
XP_011510032.1:p.Gly26352=
|
|
XM_011511731.1:c.78915A>G
(TTN)
|
XP_011510033.1:p.Gly26305=
|
|
XM_017004819.1:c.104958A>G
(TTN)
|
XP_016860308.1:p.Gly34986=
|
|
XM_017004820.1:c.100356A>G
(TTN)
|
XP_016860309.1:p.Gly33452=
|
|
XM_017004821.1:c.100353A>G
(TTN)
|
XP_016860310.1:p.Gly33451=
|
|
XM_017004822.1:c.97395A>G
(TTN)
|
XP_016860311.1:p.Gly32465=
|
|
XM_017004823.1:c.79011A>G
(TTN)
|
XP_016860312.1:p.Gly26337=
|
|
XM_024453094.1:c.100506A>G
(TTN)
|
XP_024308862.1:p.Gly33502=
|
|
XM_024453095.1:c.100503A>G
(TTN)
|
XP_024308863.1:p.Gly33501=
|
|
XM_024453096.1:c.99936A>G
(TTN)
|
XP_024308864.1:p.Gly33312=
|
|
XM_024453097.1:c.97278A>G
(TTN)
|
XP_024308865.1:p.Gly32426=
|
|
XM_024453098.1:c.97197A>G
(TTN)
|
XP_024308866.1:p.Gly32399=
|
|
XM_024453099.1:c.78960A>G
(TTN)
|
XP_024308867.1:p.Gly26320=
|
|
XM_024453100.1:c.68814A>G
(TTN)
|
XP_024308868.1:p.Gly22938=
|
|