ENST00000342992.11:c.69691G>T
(TTN)
|
ENSP00000343764.6:p.Asp23231Tyr
|
|
ENST00000342175.11:c.50776G>T
(TTN)
|
ENSP00000340554.6:p.Asp16926Tyr
|
|
ENST00000359218.10:c.50575G>T
(TTN)
|
ENSP00000352154.5:p.Asp16859Tyr
|
|
ENST00000342175.10:c.50776G>T
(TTN)
|
ENSP00000340554.6:p.Asp16926Tyr
|
|
ENST00000342992.10:c.69691G>T
(TTN)
|
ENSP00000343764.6:p.Asp23231Tyr
|
|
ENST00000359218.9:c.50575G>T
(TTN)
|
ENSP00000352154.5:p.Asp16859Tyr
|
|
ENST00000460472.6:c.50200G>T
(TTN)
|
ENSP00000434586.1:p.Asp16734Tyr
|
|
ENST00000589042.5:c.77395G>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp25799Tyr
|
|
ENST00000591111.5:c.72472G>T
(TTN)
|
ENSP00000465570.1:p.Asp24158Tyr
|
|
ENST00000615779.4:c.72472G>T
(TTN)
|
ENSP00000483597.1:p.Asp24158Tyr
|
|
NM_001256850.1:c.72472G>T
(TTN)
|
NP_001243779.1:p.Asp24158Tyr
|
|
NM_001267550.2:c.77395G>T
(TTN)
MANE Select
|
NP_001254479.2:p.Asp25799Tyr
|
|
NM_003319.4:c.50200G>T
(TTN)
|
NP_003310.4:p.Asp16734Tyr
|
|
NM_133378.4:c.69691G>T
(TTN)
|
NP_596869.4:p.Asp23231Tyr
|
|
NM_133432.3:c.50575G>T
(TTN)
|
NP_597676.3:p.Asp16859Tyr
|
|
NM_133437.4:c.50776G>T
(TTN)
|
NP_597681.4:p.Asp16926Tyr
|
|
NR_038271.1:n.447-2563C>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-13835C>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.76492G>T
(TTN)
|
XP_011510031.1:p.Asp25498Tyr
|
|
XM_011511730.1:c.50386G>T
(TTN)
|
XP_011510032.1:p.Asp16796Tyr
|
|
XM_011511731.1:c.50245G>T
(TTN)
|
XP_011510033.1:p.Asp16749Tyr
|
|
XM_017004819.1:c.76288G>T
(TTN)
|
XP_016860308.1:p.Asp25430Tyr
|
|
XM_017004820.1:c.71686G>T
(TTN)
|
XP_016860309.1:p.Asp23896Tyr
|
|
XM_017004821.1:c.71683G>T
(TTN)
|
XP_016860310.1:p.Asp23895Tyr
|
|
XM_017004822.1:c.68725G>T
(TTN)
|
XP_016860311.1:p.Asp22909Tyr
|
|
XM_017004823.1:c.50341G>T
(TTN)
|
XP_016860312.1:p.Asp16781Tyr
|
|
XM_024453094.1:c.71836G>T
(TTN)
|
XP_024308862.1:p.Asp23946Tyr
|
|
XM_024453095.1:c.71833G>T
(TTN)
|
XP_024308863.1:p.Asp23945Tyr
|
|
XM_024453096.1:c.71266G>T
(TTN)
|
XP_024308864.1:p.Asp23756Tyr
|
|
XM_024453097.1:c.68608G>T
(TTN)
|
XP_024308865.1:p.Asp22870Tyr
|
|
XM_024453098.1:c.68527G>T
(TTN)
|
XP_024308866.1:p.Asp22843Tyr
|
|
XM_024453099.1:c.50290G>T
(TTN)
|
XP_024308867.1:p.Asp16764Tyr
|
|
XM_024453100.1:c.40144G>T
(TTN)
|
XP_024308868.1:p.Asp13382Tyr
|
|