ENST00000342992.11:c.100265C>A
(TTN)
|
ENSP00000343764.6:p.Ser33422Tyr
|
|
ENST00000342175.11:c.81350C>A
(TTN)
|
ENSP00000340554.6:p.Ser27117Tyr
|
|
ENST00000359218.10:c.81149C>A
(TTN)
|
ENSP00000352154.5:p.Ser27050Tyr
|
|
ENST00000342175.10:c.81350C>A
(TTN)
|
ENSP00000340554.6:p.Ser27117Tyr
|
|
ENST00000342992.10:c.100265C>A
(TTN)
|
ENSP00000343764.6:p.Ser33422Tyr
|
|
ENST00000359218.9:c.81149C>A
(TTN)
|
ENSP00000352154.5:p.Ser27050Tyr
|
|
ENST00000460472.6:c.80774C>A
(TTN)
|
ENSP00000434586.1:p.Ser26925Tyr
|
|
ENST00000589042.5:c.107969C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ser35990Tyr
|
|
ENST00000591111.5:c.103046C>A
(TTN)
|
ENSP00000465570.1:p.Ser34349Tyr
|
|
ENST00000615779.4:c.103046C>A
(TTN)
|
ENSP00000483597.1:p.Ser34349Tyr
|
|
NM_001256850.1:c.103046C>A
(TTN)
|
NP_001243779.1:p.Ser34349Tyr
|
|
NM_001267550.2:c.107969C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Ser35990Tyr
|
|
NM_003319.4:c.80774C>A
(TTN)
|
NP_003310.4:p.Ser26925Tyr
|
|
NM_133378.4:c.100265C>A
(TTN)
|
NP_596869.4:p.Ser33422Tyr
|
|
NM_133432.3:c.81149C>A
(TTN)
|
NP_597676.3:p.Ser27050Tyr
|
|
NM_133437.4:c.81350C>A
(TTN)
|
NP_597681.4:p.Ser27117Tyr
|
|
NR_038271.1:n.446+3383G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.219+3383G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.107066C>A
(TTN)
|
XP_011510031.1:p.Ser35689Tyr
|
|
XM_011511730.1:c.80960C>A
(TTN)
|
XP_011510032.1:p.Ser26987Tyr
|
|
XM_011511731.1:c.80819C>A
(TTN)
|
XP_011510033.1:p.Ser26940Tyr
|
|
XM_017004819.1:c.106862C>A
(TTN)
|
XP_016860308.1:p.Ser35621Tyr
|
|
XM_017004820.1:c.102260C>A
(TTN)
|
XP_016860309.1:p.Ser34087Tyr
|
|
XM_017004821.1:c.102257C>A
(TTN)
|
XP_016860310.1:p.Ser34086Tyr
|
|
XM_017004822.1:c.99299C>A
(TTN)
|
XP_016860311.1:p.Ser33100Tyr
|
|
XM_017004823.1:c.80915C>A
(TTN)
|
XP_016860312.1:p.Ser26972Tyr
|
|
XM_024453094.1:c.102410C>A
(TTN)
|
XP_024308862.1:p.Ser34137Tyr
|
|
XM_024453095.1:c.102407C>A
(TTN)
|
XP_024308863.1:p.Ser34136Tyr
|
|
XM_024453096.1:c.101840C>A
(TTN)
|
XP_024308864.1:p.Ser33947Tyr
|
|
XM_024453097.1:c.99182C>A
(TTN)
|
XP_024308865.1:p.Ser33061Tyr
|
|
XM_024453098.1:c.99101C>A
(TTN)
|
XP_024308866.1:p.Ser33034Tyr
|
|
XM_024453099.1:c.80864C>A
(TTN)
|
XP_024308867.1:p.Ser26955Tyr
|
|
XM_024453100.1:c.70718C>A
(TTN)
|
XP_024308868.1:p.Ser23573Tyr
|
|