ENST00000342992.11:c.88154C>A
(TTN)
|
ENSP00000343764.6:p.Thr29385Asn
|
|
ENST00000342175.11:c.69239C>A
(TTN)
|
ENSP00000340554.6:p.Thr23080Asn
|
|
ENST00000359218.10:c.69038C>A
(TTN)
|
ENSP00000352154.5:p.Thr23013Asn
|
|
ENST00000342175.10:c.69239C>A
(TTN)
|
ENSP00000340554.6:p.Thr23080Asn
|
|
ENST00000342992.10:c.88154C>A
(TTN)
|
ENSP00000343764.6:p.Thr29385Asn
|
|
ENST00000359218.9:c.69038C>A
(TTN)
|
ENSP00000352154.5:p.Thr23013Asn
|
|
ENST00000460472.6:c.68663C>A
(TTN)
|
ENSP00000434586.1:p.Thr22888Asn
|
|
ENST00000589042.5:c.95858C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr31953Asn
|
|
ENST00000591111.5:c.90935C>A
(TTN)
|
ENSP00000465570.1:p.Thr30312Asn
|
|
ENST00000615779.4:c.90935C>A
(TTN)
|
ENSP00000483597.1:p.Thr30312Asn
|
|
NM_001256850.1:c.90935C>A
(TTN)
|
NP_001243779.1:p.Thr30312Asn
|
|
NM_001267550.2:c.95858C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Thr31953Asn
|
|
NM_003319.4:c.68663C>A
(TTN)
|
NP_003310.4:p.Thr22888Asn
|
|
NM_133378.4:c.88154C>A
(TTN)
|
NP_596869.4:p.Thr29385Asn
|
|
NM_133432.3:c.69038C>A
(TTN)
|
NP_597676.3:p.Thr23013Asn
|
|
NM_133437.4:c.69239C>A
(TTN)
|
NP_597681.4:p.Thr23080Asn
|
|
NR_038271.1:n.446+20735G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+2010G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.94955C>A
(TTN)
|
XP_011510031.1:p.Thr31652Asn
|
|
XM_011511730.1:c.68849C>A
(TTN)
|
XP_011510032.1:p.Thr22950Asn
|
|
XM_011511731.1:c.68708C>A
(TTN)
|
XP_011510033.1:p.Thr22903Asn
|
|
XM_017004819.1:c.94751C>A
(TTN)
|
XP_016860308.1:p.Thr31584Asn
|
|
XM_017004820.1:c.90149C>A
(TTN)
|
XP_016860309.1:p.Thr30050Asn
|
|
XM_017004821.1:c.90146C>A
(TTN)
|
XP_016860310.1:p.Thr30049Asn
|
|
XM_017004822.1:c.87188C>A
(TTN)
|
XP_016860311.1:p.Thr29063Asn
|
|
XM_017004823.1:c.68804C>A
(TTN)
|
XP_016860312.1:p.Thr22935Asn
|
|
XM_024453094.1:c.90299C>A
(TTN)
|
XP_024308862.1:p.Thr30100Asn
|
|
XM_024453095.1:c.90296C>A
(TTN)
|
XP_024308863.1:p.Thr30099Asn
|
|
XM_024453096.1:c.89729C>A
(TTN)
|
XP_024308864.1:p.Thr29910Asn
|
|
XM_024453097.1:c.87071C>A
(TTN)
|
XP_024308865.1:p.Thr29024Asn
|
|
XM_024453098.1:c.86990C>A
(TTN)
|
XP_024308866.1:p.Thr28997Asn
|
|
XM_024453099.1:c.68753C>A
(TTN)
|
XP_024308867.1:p.Thr22918Asn
|
|
XM_024453100.1:c.58607C>A
(TTN)
|
XP_024308868.1:p.Thr19536Asn
|
|