ENST00000342992.11:c.91870G>T
(TTN)
|
ENSP00000343764.6:p.Ala30624Ser
|
|
ENST00000342175.11:c.72955G>T
(TTN)
|
ENSP00000340554.6:p.Ala24319Ser
|
|
ENST00000359218.10:c.72754G>T
(TTN)
|
ENSP00000352154.5:p.Ala24252Ser
|
|
ENST00000342175.10:c.72955G>T
(TTN)
|
ENSP00000340554.6:p.Ala24319Ser
|
|
ENST00000342992.10:c.91870G>T
(TTN)
|
ENSP00000343764.6:p.Ala30624Ser
|
|
ENST00000359218.9:c.72754G>T
(TTN)
|
ENSP00000352154.5:p.Ala24252Ser
|
|
ENST00000460472.6:c.72379G>T
(TTN)
|
ENSP00000434586.1:p.Ala24127Ser
|
|
ENST00000589042.5:c.99574G>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ala33192Ser
|
|
ENST00000591111.5:c.94651G>T
(TTN)
|
ENSP00000465570.1:p.Ala31551Ser
|
|
ENST00000615779.4:c.94651G>T
(TTN)
|
ENSP00000483597.1:p.Ala31551Ser
|
|
NM_001256850.1:c.94651G>T
(TTN)
|
NP_001243779.1:p.Ala31551Ser
|
|
NM_001267550.2:c.99574G>T
(TTN)
MANE Select
|
NP_001254479.2:p.Ala33192Ser
|
|
NM_003319.4:c.72379G>T
(TTN)
|
NP_003310.4:p.Ala24127Ser
|
|
NM_133378.4:c.91870G>T
(TTN)
|
NP_596869.4:p.Ala30624Ser
|
|
NM_133432.3:c.72754G>T
(TTN)
|
NP_597676.3:p.Ala24252Ser
|
|
NM_133437.4:c.72955G>T
(TTN)
|
NP_597681.4:p.Ala24319Ser
|
|
NR_038271.1:n.446+13997C>A
(TTN-AS1)
|
|
|
NR_038272.1:n.589C>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.98671G>T
(TTN)
|
XP_011510031.1:p.Ala32891Ser
|
|
XM_011511730.1:c.72565G>T
(TTN)
|
XP_011510032.1:p.Ala24189Ser
|
|
XM_011511731.1:c.72424G>T
(TTN)
|
XP_011510033.1:p.Ala24142Ser
|
|
XM_017004819.1:c.98467G>T
(TTN)
|
XP_016860308.1:p.Ala32823Ser
|
|
XM_017004820.1:c.93865G>T
(TTN)
|
XP_016860309.1:p.Ala31289Ser
|
|
XM_017004821.1:c.93862G>T
(TTN)
|
XP_016860310.1:p.Ala31288Ser
|
|
XM_017004822.1:c.90904G>T
(TTN)
|
XP_016860311.1:p.Ala30302Ser
|
|
XM_017004823.1:c.72520G>T
(TTN)
|
XP_016860312.1:p.Ala24174Ser
|
|
XM_024453094.1:c.94015G>T
(TTN)
|
XP_024308862.1:p.Ala31339Ser
|
|
XM_024453095.1:c.94012G>T
(TTN)
|
XP_024308863.1:p.Ala31338Ser
|
|
XM_024453096.1:c.93445G>T
(TTN)
|
XP_024308864.1:p.Ala31149Ser
|
|
XM_024453097.1:c.90787G>T
(TTN)
|
XP_024308865.1:p.Ala30263Ser
|
|
XM_024453098.1:c.90706G>T
(TTN)
|
XP_024308866.1:p.Ala30236Ser
|
|
XM_024453099.1:c.72469G>T
(TTN)
|
XP_024308867.1:p.Ala24157Ser
|
|
XM_024453100.1:c.62323G>T
(TTN)
|
XP_024308868.1:p.Ala20775Ser
|
|