ENST00000342992.11:c.96685G>A
(TTN)
|
ENSP00000343764.6:p.Glu32229Lys
|
|
ENST00000342175.11:c.77770G>A
(TTN)
|
ENSP00000340554.6:p.Glu25924Lys
|
|
ENST00000359218.10:c.77569G>A
(TTN)
|
ENSP00000352154.5:p.Glu25857Lys
|
|
ENST00000342175.10:c.77770G>A
(TTN)
|
ENSP00000340554.6:p.Glu25924Lys
|
|
ENST00000342992.10:c.96685G>A
(TTN)
|
ENSP00000343764.6:p.Glu32229Lys
|
|
ENST00000359218.9:c.77569G>A
(TTN)
|
ENSP00000352154.5:p.Glu25857Lys
|
|
ENST00000460472.6:c.77194G>A
(TTN)
|
ENSP00000434586.1:p.Glu25732Lys
|
|
ENST00000589042.5:c.104389G>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu34797Lys
|
|
ENST00000591111.5:c.99466G>A
(TTN)
|
ENSP00000465570.1:p.Glu33156Lys
|
|
ENST00000615779.4:c.99466G>A
(TTN)
|
ENSP00000483597.1:p.Glu33156Lys
|
|
NM_001256850.1:c.99466G>A
(TTN)
|
NP_001243779.1:p.Glu33156Lys
|
|
NM_001267550.2:c.104389G>A
(TTN)
MANE Select
|
NP_001254479.2:p.Glu34797Lys
|
|
NM_003319.4:c.77194G>A
(TTN)
|
NP_003310.4:p.Glu25732Lys
|
|
NM_133378.4:c.96685G>A
(TTN)
|
NP_596869.4:p.Glu32229Lys
|
|
NM_133432.3:c.77569G>A
(TTN)
|
NP_597676.3:p.Glu25857Lys
|
|
NM_133437.4:c.77770G>A
(TTN)
|
NP_597681.4:p.Glu25924Lys
|
|
NR_038271.1:n.446+8590C>T
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3506C>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.103486G>A
(TTN)
|
XP_011510031.1:p.Glu34496Lys
|
|
XM_011511730.1:c.77380G>A
(TTN)
|
XP_011510032.1:p.Glu25794Lys
|
|
XM_011511731.1:c.77239G>A
(TTN)
|
XP_011510033.1:p.Glu25747Lys
|
|
XM_017004819.1:c.103282G>A
(TTN)
|
XP_016860308.1:p.Glu34428Lys
|
|
XM_017004820.1:c.98680G>A
(TTN)
|
XP_016860309.1:p.Glu32894Lys
|
|
XM_017004821.1:c.98677G>A
(TTN)
|
XP_016860310.1:p.Glu32893Lys
|
|
XM_017004822.1:c.95719G>A
(TTN)
|
XP_016860311.1:p.Glu31907Lys
|
|
XM_017004823.1:c.77335G>A
(TTN)
|
XP_016860312.1:p.Glu25779Lys
|
|
XM_024453094.1:c.98830G>A
(TTN)
|
XP_024308862.1:p.Glu32944Lys
|
|
XM_024453095.1:c.98827G>A
(TTN)
|
XP_024308863.1:p.Glu32943Lys
|
|
XM_024453096.1:c.98260G>A
(TTN)
|
XP_024308864.1:p.Glu32754Lys
|
|
XM_024453097.1:c.95602G>A
(TTN)
|
XP_024308865.1:p.Glu31868Lys
|
|
XM_024453098.1:c.95521G>A
(TTN)
|
XP_024308866.1:p.Glu31841Lys
|
|
XM_024453099.1:c.77284G>A
(TTN)
|
XP_024308867.1:p.Glu25762Lys
|
|
XM_024453100.1:c.67138G>A
(TTN)
|
XP_024308868.1:p.Glu22380Lys
|
|