ENST00000342992.11:c.82721C>G
(TTN)
|
ENSP00000343764.6:p.Thr27574Ser
|
|
ENST00000342175.11:c.63806C>G
(TTN)
|
ENSP00000340554.6:p.Thr21269Ser
|
|
ENST00000359218.10:c.63605C>G
(TTN)
|
ENSP00000352154.5:p.Thr21202Ser
|
|
ENST00000342175.10:c.63806C>G
(TTN)
|
ENSP00000340554.6:p.Thr21269Ser
|
|
ENST00000342992.10:c.82721C>G
(TTN)
|
ENSP00000343764.6:p.Thr27574Ser
|
|
ENST00000359218.9:c.63605C>G
(TTN)
|
ENSP00000352154.5:p.Thr21202Ser
|
|
ENST00000460472.6:c.63230C>G
(TTN)
|
ENSP00000434586.1:p.Thr21077Ser
|
|
ENST00000589042.5:c.90425C>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr30142Ser
|
|
ENST00000591111.5:c.85502C>G
(TTN)
|
ENSP00000465570.1:p.Thr28501Ser
|
|
ENST00000615779.4:c.85502C>G
(TTN)
|
ENSP00000483597.1:p.Thr28501Ser
|
|
NM_001256850.1:c.85502C>G
(TTN)
|
NP_001243779.1:p.Thr28501Ser
|
|
NM_001267550.2:c.90425C>G
(TTN)
MANE Select
|
NP_001254479.2:p.Thr30142Ser
|
|
NM_003319.4:c.63230C>G
(TTN)
|
NP_003310.4:p.Thr21077Ser
|
|
NM_133378.4:c.82721C>G
(TTN)
|
NP_596869.4:p.Thr27574Ser
|
|
NM_133432.3:c.63605C>G
(TTN)
|
NP_597676.3:p.Thr21202Ser
|
|
NM_133437.4:c.63806C>G
(TTN)
|
NP_597681.4:p.Thr21269Ser
|
|
NR_038271.1:n.447-18825G>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+10114G>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.89522C>G
(TTN)
|
XP_011510031.1:p.Thr29841Ser
|
|
XM_011511730.1:c.63416C>G
(TTN)
|
XP_011510032.1:p.Thr21139Ser
|
|
XM_011511731.1:c.63275C>G
(TTN)
|
XP_011510033.1:p.Thr21092Ser
|
|
XM_017004819.1:c.89318C>G
(TTN)
|
XP_016860308.1:p.Thr29773Ser
|
|
XM_017004820.1:c.84716C>G
(TTN)
|
XP_016860309.1:p.Thr28239Ser
|
|
XM_017004821.1:c.84713C>G
(TTN)
|
XP_016860310.1:p.Thr28238Ser
|
|
XM_017004822.1:c.81755C>G
(TTN)
|
XP_016860311.1:p.Thr27252Ser
|
|
XM_017004823.1:c.63371C>G
(TTN)
|
XP_016860312.1:p.Thr21124Ser
|
|
XM_024453094.1:c.84866C>G
(TTN)
|
XP_024308862.1:p.Thr28289Ser
|
|
XM_024453095.1:c.84863C>G
(TTN)
|
XP_024308863.1:p.Thr28288Ser
|
|
XM_024453096.1:c.84296C>G
(TTN)
|
XP_024308864.1:p.Thr28099Ser
|
|
XM_024453097.1:c.81638C>G
(TTN)
|
XP_024308865.1:p.Thr27213Ser
|
|
XM_024453098.1:c.81557C>G
(TTN)
|
XP_024308866.1:p.Thr27186Ser
|
|
XM_024453099.1:c.63320C>G
(TTN)
|
XP_024308867.1:p.Thr21107Ser
|
|
XM_024453100.1:c.53174C>G
(TTN)
|
XP_024308868.1:p.Thr17725Ser
|
|