ENST00000342992.11:c.88199C>A
(TTN)
|
ENSP00000343764.6:p.Thr29400Asn
|
|
ENST00000342175.11:c.69284C>A
(TTN)
|
ENSP00000340554.6:p.Thr23095Asn
|
|
ENST00000359218.10:c.69083C>A
(TTN)
|
ENSP00000352154.5:p.Thr23028Asn
|
|
ENST00000342175.10:c.69284C>A
(TTN)
|
ENSP00000340554.6:p.Thr23095Asn
|
|
ENST00000342992.10:c.88199C>A
(TTN)
|
ENSP00000343764.6:p.Thr29400Asn
|
|
ENST00000359218.9:c.69083C>A
(TTN)
|
ENSP00000352154.5:p.Thr23028Asn
|
|
ENST00000460472.6:c.68708C>A
(TTN)
|
ENSP00000434586.1:p.Thr22903Asn
|
|
ENST00000589042.5:c.95903C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr31968Asn
|
|
ENST00000591111.5:c.90980C>A
(TTN)
|
ENSP00000465570.1:p.Thr30327Asn
|
|
ENST00000615779.4:c.90980C>A
(TTN)
|
ENSP00000483597.1:p.Thr30327Asn
|
|
NM_001256850.1:c.90980C>A
(TTN)
|
NP_001243779.1:p.Thr30327Asn
|
|
NM_001267550.2:c.95903C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Thr31968Asn
|
|
NM_003319.4:c.68708C>A
(TTN)
|
NP_003310.4:p.Thr22903Asn
|
|
NM_133378.4:c.88199C>A
(TTN)
|
NP_596869.4:p.Thr29400Asn
|
|
NM_133432.3:c.69083C>A
(TTN)
|
NP_597676.3:p.Thr23028Asn
|
|
NM_133437.4:c.69284C>A
(TTN)
|
NP_597681.4:p.Thr23095Asn
|
|
NR_038271.1:n.446+20690G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+1965G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.95000C>A
(TTN)
|
XP_011510031.1:p.Thr31667Asn
|
|
XM_011511730.1:c.68894C>A
(TTN)
|
XP_011510032.1:p.Thr22965Asn
|
|
XM_011511731.1:c.68753C>A
(TTN)
|
XP_011510033.1:p.Thr22918Asn
|
|
XM_017004819.1:c.94796C>A
(TTN)
|
XP_016860308.1:p.Thr31599Asn
|
|
XM_017004820.1:c.90194C>A
(TTN)
|
XP_016860309.1:p.Thr30065Asn
|
|
XM_017004821.1:c.90191C>A
(TTN)
|
XP_016860310.1:p.Thr30064Asn
|
|
XM_017004822.1:c.87233C>A
(TTN)
|
XP_016860311.1:p.Thr29078Asn
|
|
XM_017004823.1:c.68849C>A
(TTN)
|
XP_016860312.1:p.Thr22950Asn
|
|
XM_024453094.1:c.90344C>A
(TTN)
|
XP_024308862.1:p.Thr30115Asn
|
|
XM_024453095.1:c.90341C>A
(TTN)
|
XP_024308863.1:p.Thr30114Asn
|
|
XM_024453096.1:c.89774C>A
(TTN)
|
XP_024308864.1:p.Thr29925Asn
|
|
XM_024453097.1:c.87116C>A
(TTN)
|
XP_024308865.1:p.Thr29039Asn
|
|
XM_024453098.1:c.87035C>A
(TTN)
|
XP_024308866.1:p.Thr29012Asn
|
|
XM_024453099.1:c.68798C>A
(TTN)
|
XP_024308867.1:p.Thr22933Asn
|
|
XM_024453100.1:c.58652C>A
(TTN)
|
XP_024308868.1:p.Thr19551Asn
|
|