ENST00000342992.11:c.62437G>A
(TTN)
|
ENSP00000343764.6:p.Asp20813Asn
|
|
ENST00000342175.11:c.43522G>A
(TTN)
|
ENSP00000340554.6:p.Asp14508Asn
|
|
ENST00000359218.10:c.43321G>A
(TTN)
|
ENSP00000352154.5:p.Asp14441Asn
|
|
ENST00000342175.10:c.43522G>A
(TTN)
|
ENSP00000340554.6:p.Asp14508Asn
|
|
ENST00000342992.10:c.62437G>A
(TTN)
|
ENSP00000343764.6:p.Asp20813Asn
|
|
ENST00000359218.9:c.43321G>A
(TTN)
|
ENSP00000352154.5:p.Asp14441Asn
|
|
ENST00000460472.6:c.42946G>A
(TTN)
|
ENSP00000434586.1:p.Asp14316Asn
|
|
ENST00000589042.5:c.70141G>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp23381Asn
|
|
ENST00000591111.5:c.65218G>A
(TTN)
|
ENSP00000465570.1:p.Asp21740Asn
|
|
ENST00000615779.4:c.65218G>A
(TTN)
|
ENSP00000483597.1:p.Asp21740Asn
|
|
NM_001256850.1:c.65218G>A
(TTN)
|
NP_001243779.1:p.Asp21740Asn
|
|
NM_001267550.2:c.70141G>A
(TTN)
MANE Select
|
NP_001254479.2:p.Asp23381Asn
|
|
NM_003319.4:c.42946G>A
(TTN)
|
NP_003310.4:p.Asp14316Asn
|
|
NM_133378.4:c.62437G>A
(TTN)
|
NP_596869.4:p.Asp20813Asn
|
|
NM_133432.3:c.43321G>A
(TTN)
|
NP_597676.3:p.Asp14441Asn
|
|
NM_133437.4:c.43522G>A
(TTN)
|
NP_597681.4:p.Asp14508Asn
|
|
NR_038271.1:n.596+4542C>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-6581C>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.69238G>A
(TTN)
|
XP_011510031.1:p.Asp23080Asn
|
|
XM_011511730.1:c.43132G>A
(TTN)
|
XP_011510032.1:p.Asp14378Asn
|
|
XM_011511731.1:c.42991G>A
(TTN)
|
XP_011510033.1:p.Asp14331Asn
|
|
XM_017004819.1:c.69034G>A
(TTN)
|
XP_016860308.1:p.Asp23012Asn
|
|
XM_017004820.1:c.64432G>A
(TTN)
|
XP_016860309.1:p.Asp21478Asn
|
|
XM_017004821.1:c.64429G>A
(TTN)
|
XP_016860310.1:p.Asp21477Asn
|
|
XM_017004822.1:c.61471G>A
(TTN)
|
XP_016860311.1:p.Asp20491Asn
|
|
XM_017004823.1:c.43087G>A
(TTN)
|
XP_016860312.1:p.Asp14363Asn
|
|
XM_024453094.1:c.64582G>A
(TTN)
|
XP_024308862.1:p.Asp21528Asn
|
|
XM_024453095.1:c.64579G>A
(TTN)
|
XP_024308863.1:p.Asp21527Asn
|
|
XM_024453096.1:c.64012G>A
(TTN)
|
XP_024308864.1:p.Asp21338Asn
|
|
XM_024453097.1:c.61354G>A
(TTN)
|
XP_024308865.1:p.Asp20452Asn
|
|
XM_024453098.1:c.61273G>A
(TTN)
|
XP_024308866.1:p.Asp20425Asn
|
|
XM_024453099.1:c.43036G>A
(TTN)
|
XP_024308867.1:p.Asp14346Asn
|
|
XM_024453100.1:c.32890G>A
(TTN)
|
XP_024308868.1:p.Asp10964Asn
|
|