ENST00000342992.11:c.87654C>A
(TTN)
|
ENSP00000343764.6:p.Asn29218Lys
|
|
ENST00000342175.11:c.68739C>A
(TTN)
|
ENSP00000340554.6:p.Asn22913Lys
|
|
ENST00000359218.10:c.68538C>A
(TTN)
|
ENSP00000352154.5:p.Asn22846Lys
|
|
ENST00000342175.10:c.68739C>A
(TTN)
|
ENSP00000340554.6:p.Asn22913Lys
|
|
ENST00000342992.10:c.87654C>A
(TTN)
|
ENSP00000343764.6:p.Asn29218Lys
|
|
ENST00000359218.9:c.68538C>A
(TTN)
|
ENSP00000352154.5:p.Asn22846Lys
|
|
ENST00000460472.6:c.68163C>A
(TTN)
|
ENSP00000434586.1:p.Asn22721Lys
|
|
ENST00000589042.5:c.95358C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asn31786Lys
|
|
ENST00000591111.5:c.90435C>A
(TTN)
|
ENSP00000465570.1:p.Asn30145Lys
|
|
ENST00000615779.4:c.90435C>A
(TTN)
|
ENSP00000483597.1:p.Asn30145Lys
|
|
NM_001256850.1:c.90435C>A
(TTN)
|
NP_001243779.1:p.Asn30145Lys
|
|
NM_001267550.2:c.95358C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Asn31786Lys
|
|
NM_003319.4:c.68163C>A
(TTN)
|
NP_003310.4:p.Asn22721Lys
|
|
NM_133378.4:c.87654C>A
(TTN)
|
NP_596869.4:p.Asn29218Lys
|
|
NM_133432.3:c.68538C>A
(TTN)
|
NP_597676.3:p.Asn22846Lys
|
|
NM_133437.4:c.68739C>A
(TTN)
|
NP_597681.4:p.Asn22913Lys
|
|
NR_038271.1:n.446+22242G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+3517G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.94455C>A
(TTN)
|
XP_011510031.1:p.Asn31485Lys
|
|
XM_011511730.1:c.68349C>A
(TTN)
|
XP_011510032.1:p.Asn22783Lys
|
|
XM_011511731.1:c.68208C>A
(TTN)
|
XP_011510033.1:p.Asn22736Lys
|
|
XM_017004819.1:c.94251C>A
(TTN)
|
XP_016860308.1:p.Asn31417Lys
|
|
XM_017004820.1:c.89649C>A
(TTN)
|
XP_016860309.1:p.Asn29883Lys
|
|
XM_017004821.1:c.89646C>A
(TTN)
|
XP_016860310.1:p.Asn29882Lys
|
|
XM_017004822.1:c.86688C>A
(TTN)
|
XP_016860311.1:p.Asn28896Lys
|
|
XM_017004823.1:c.68304C>A
(TTN)
|
XP_016860312.1:p.Asn22768Lys
|
|
XM_024453094.1:c.89799C>A
(TTN)
|
XP_024308862.1:p.Asn29933Lys
|
|
XM_024453095.1:c.89796C>A
(TTN)
|
XP_024308863.1:p.Asn29932Lys
|
|
XM_024453096.1:c.89229C>A
(TTN)
|
XP_024308864.1:p.Asn29743Lys
|
|
XM_024453097.1:c.86571C>A
(TTN)
|
XP_024308865.1:p.Asn28857Lys
|
|
XM_024453098.1:c.86490C>A
(TTN)
|
XP_024308866.1:p.Asn28830Lys
|
|
XM_024453099.1:c.68253C>A
(TTN)
|
XP_024308867.1:p.Asn22751Lys
|
|
XM_024453100.1:c.58107C>A
(TTN)
|
XP_024308868.1:p.Asn19369Lys
|
|