ENST00000342992.11:c.96693T>C
(TTN)
|
ENSP00000343764.6:p.Ser32231=
|
|
ENST00000342175.11:c.77778T>C
(TTN)
|
ENSP00000340554.6:p.Ser25926=
|
|
ENST00000359218.10:c.77577T>C
(TTN)
|
ENSP00000352154.5:p.Ser25859=
|
|
ENST00000342175.10:c.77778T>C
(TTN)
|
ENSP00000340554.6:p.Ser25926=
|
|
ENST00000342992.10:c.96693T>C
(TTN)
|
ENSP00000343764.6:p.Ser32231=
|
|
ENST00000359218.9:c.77577T>C
(TTN)
|
ENSP00000352154.5:p.Ser25859=
|
|
ENST00000460472.6:c.77202T>C
(TTN)
|
ENSP00000434586.1:p.Ser25734=
|
|
ENST00000589042.5:c.104397T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ser34799=
|
|
ENST00000591111.5:c.99474T>C
(TTN)
|
ENSP00000465570.1:p.Ser33158=
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ENST00000615779.4:c.99474T>C
(TTN)
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ENSP00000483597.1:p.Ser33158=
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|
NM_001256850.1:c.99474T>C
(TTN)
|
NP_001243779.1:p.Ser33158=
|
|
NM_001267550.2:c.104397T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Ser34799=
|
|
NM_003319.4:c.77202T>C
(TTN)
|
NP_003310.4:p.Ser25734=
|
|
NM_133378.4:c.96693T>C
(TTN)
|
NP_596869.4:p.Ser32231=
|
|
NM_133432.3:c.77577T>C
(TTN)
|
NP_597676.3:p.Ser25859=
|
|
NM_133437.4:c.77778T>C
(TTN)
|
NP_597681.4:p.Ser25926=
|
|
NR_038271.1:n.446+8582A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3514A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.103494T>C
(TTN)
|
XP_011510031.1:p.Ser34498=
|
|
XM_011511730.1:c.77388T>C
(TTN)
|
XP_011510032.1:p.Ser25796=
|
|
XM_011511731.1:c.77247T>C
(TTN)
|
XP_011510033.1:p.Ser25749=
|
|
XM_017004819.1:c.103290T>C
(TTN)
|
XP_016860308.1:p.Ser34430=
|
|
XM_017004820.1:c.98688T>C
(TTN)
|
XP_016860309.1:p.Ser32896=
|
|
XM_017004821.1:c.98685T>C
(TTN)
|
XP_016860310.1:p.Ser32895=
|
|
XM_017004822.1:c.95727T>C
(TTN)
|
XP_016860311.1:p.Ser31909=
|
|
XM_017004823.1:c.77343T>C
(TTN)
|
XP_016860312.1:p.Ser25781=
|
|
XM_024453094.1:c.98838T>C
(TTN)
|
XP_024308862.1:p.Ser32946=
|
|
XM_024453095.1:c.98835T>C
(TTN)
|
XP_024308863.1:p.Ser32945=
|
|
XM_024453096.1:c.98268T>C
(TTN)
|
XP_024308864.1:p.Ser32756=
|
|
XM_024453097.1:c.95610T>C
(TTN)
|
XP_024308865.1:p.Ser31870=
|
|
XM_024453098.1:c.95529T>C
(TTN)
|
XP_024308866.1:p.Ser31843=
|
|
XM_024453099.1:c.77292T>C
(TTN)
|
XP_024308867.1:p.Ser25764=
|
|
XM_024453100.1:c.67146T>C
(TTN)
|
XP_024308868.1:p.Ser22382=
|
|