ENST00000342992.11:c.96645C>A
(TTN)
|
ENSP00000343764.6:p.Leu32215=
|
|
ENST00000342175.11:c.77730C>A
(TTN)
|
ENSP00000340554.6:p.Leu25910=
|
|
ENST00000359218.10:c.77529C>A
(TTN)
|
ENSP00000352154.5:p.Leu25843=
|
|
ENST00000342175.10:c.77730C>A
(TTN)
|
ENSP00000340554.6:p.Leu25910=
|
|
ENST00000342992.10:c.96645C>A
(TTN)
|
ENSP00000343764.6:p.Leu32215=
|
|
ENST00000359218.9:c.77529C>A
(TTN)
|
ENSP00000352154.5:p.Leu25843=
|
|
ENST00000460472.6:c.77154C>A
(TTN)
|
ENSP00000434586.1:p.Leu25718=
|
|
ENST00000589042.5:c.104349C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu34783=
|
|
ENST00000591111.5:c.99426C>A
(TTN)
|
ENSP00000465570.1:p.Leu33142=
|
|
ENST00000615779.4:c.99426C>A
(TTN)
|
ENSP00000483597.1:p.Leu33142=
|
|
NM_001256850.1:c.99426C>A
(TTN)
|
NP_001243779.1:p.Leu33142=
|
|
NM_001267550.2:c.104349C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Leu34783=
|
|
NM_003319.4:c.77154C>A
(TTN)
|
NP_003310.4:p.Leu25718=
|
|
NM_133378.4:c.96645C>A
(TTN)
|
NP_596869.4:p.Leu32215=
|
|
NM_133432.3:c.77529C>A
(TTN)
|
NP_597676.3:p.Leu25843=
|
|
NM_133437.4:c.77730C>A
(TTN)
|
NP_597681.4:p.Leu25910=
|
|
NR_038271.1:n.446+8630G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3466G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.103446C>A
(TTN)
|
XP_011510031.1:p.Leu34482=
|
|
XM_011511730.1:c.77340C>A
(TTN)
|
XP_011510032.1:p.Leu25780=
|
|
XM_011511731.1:c.77199C>A
(TTN)
|
XP_011510033.1:p.Leu25733=
|
|
XM_017004819.1:c.103242C>A
(TTN)
|
XP_016860308.1:p.Leu34414=
|
|
XM_017004820.1:c.98640C>A
(TTN)
|
XP_016860309.1:p.Leu32880=
|
|
XM_017004821.1:c.98637C>A
(TTN)
|
XP_016860310.1:p.Leu32879=
|
|
XM_017004822.1:c.95679C>A
(TTN)
|
XP_016860311.1:p.Leu31893=
|
|
XM_017004823.1:c.77295C>A
(TTN)
|
XP_016860312.1:p.Leu25765=
|
|
XM_024453094.1:c.98790C>A
(TTN)
|
XP_024308862.1:p.Leu32930=
|
|
XM_024453095.1:c.98787C>A
(TTN)
|
XP_024308863.1:p.Leu32929=
|
|
XM_024453096.1:c.98220C>A
(TTN)
|
XP_024308864.1:p.Leu32740=
|
|
XM_024453097.1:c.95562C>A
(TTN)
|
XP_024308865.1:p.Leu31854=
|
|
XM_024453098.1:c.95481C>A
(TTN)
|
XP_024308866.1:p.Leu31827=
|
|
XM_024453099.1:c.77244C>A
(TTN)
|
XP_024308867.1:p.Leu25748=
|
|
XM_024453100.1:c.67098C>A
(TTN)
|
XP_024308868.1:p.Leu22366=
|
|