ENST00000342992.11:c.98673C>T
(TTN)
|
ENSP00000343764.6:p.Ala32891=
|
|
ENST00000342175.11:c.79758C>T
(TTN)
|
ENSP00000340554.6:p.Ala26586=
|
|
ENST00000359218.10:c.79557C>T
(TTN)
|
ENSP00000352154.5:p.Ala26519=
|
|
ENST00000342175.10:c.79758C>T
(TTN)
|
ENSP00000340554.6:p.Ala26586=
|
|
ENST00000342992.10:c.98673C>T
(TTN)
|
ENSP00000343764.6:p.Ala32891=
|
|
ENST00000359218.9:c.79557C>T
(TTN)
|
ENSP00000352154.5:p.Ala26519=
|
|
ENST00000460472.6:c.79182C>T
(TTN)
|
ENSP00000434586.1:p.Ala26394=
|
|
ENST00000589042.5:c.106377C>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ala35459=
|
|
ENST00000591111.5:c.101454C>T
(TTN)
|
ENSP00000465570.1:p.Ala33818=
|
|
ENST00000615779.4:c.101454C>T
(TTN)
|
ENSP00000483597.1:p.Ala33818=
|
|
NM_001256850.1:c.101454C>T
(TTN)
|
NP_001243779.1:p.Ala33818=
|
|
NM_001267550.2:c.106377C>T
(TTN)
MANE Select
|
NP_001254479.2:p.Ala35459=
|
|
NM_003319.4:c.79182C>T
(TTN)
|
NP_003310.4:p.Ala26394=
|
|
NM_133378.4:c.98673C>T
(TTN)
|
NP_596869.4:p.Ala32891=
|
|
NM_133432.3:c.79557C>T
(TTN)
|
NP_597676.3:p.Ala26519=
|
|
NM_133437.4:c.79758C>T
(TTN)
|
NP_597681.4:p.Ala26586=
|
|
NR_038271.1:n.446+6478G>A
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5618G>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.105474C>T
(TTN)
|
XP_011510031.1:p.Ala35158=
|
|
XM_011511730.1:c.79368C>T
(TTN)
|
XP_011510032.1:p.Ala26456=
|
|
XM_011511731.1:c.79227C>T
(TTN)
|
XP_011510033.1:p.Ala26409=
|
|
XM_017004819.1:c.105270C>T
(TTN)
|
XP_016860308.1:p.Ala35090=
|
|
XM_017004820.1:c.100668C>T
(TTN)
|
XP_016860309.1:p.Ala33556=
|
|
XM_017004821.1:c.100665C>T
(TTN)
|
XP_016860310.1:p.Ala33555=
|
|
XM_017004822.1:c.97707C>T
(TTN)
|
XP_016860311.1:p.Ala32569=
|
|
XM_017004823.1:c.79323C>T
(TTN)
|
XP_016860312.1:p.Ala26441=
|
|
XM_024453094.1:c.100818C>T
(TTN)
|
XP_024308862.1:p.Ala33606=
|
|
XM_024453095.1:c.100815C>T
(TTN)
|
XP_024308863.1:p.Ala33605=
|
|
XM_024453096.1:c.100248C>T
(TTN)
|
XP_024308864.1:p.Ala33416=
|
|
XM_024453097.1:c.97590C>T
(TTN)
|
XP_024308865.1:p.Ala32530=
|
|
XM_024453098.1:c.97509C>T
(TTN)
|
XP_024308866.1:p.Ala32503=
|
|
XM_024453099.1:c.79272C>T
(TTN)
|
XP_024308867.1:p.Ala26424=
|
|
XM_024453100.1:c.69126C>T
(TTN)
|
XP_024308868.1:p.Ala23042=
|
|