ENST00000342992.11:c.92240C>A
(TTN)
|
ENSP00000343764.6:p.Pro30747His
|
|
ENST00000342175.11:c.73325C>A
(TTN)
|
ENSP00000340554.6:p.Pro24442His
|
|
ENST00000359218.10:c.73124C>A
(TTN)
|
ENSP00000352154.5:p.Pro24375His
|
|
ENST00000342175.10:c.73325C>A
(TTN)
|
ENSP00000340554.6:p.Pro24442His
|
|
ENST00000342992.10:c.92240C>A
(TTN)
|
ENSP00000343764.6:p.Pro30747His
|
|
ENST00000359218.9:c.73124C>A
(TTN)
|
ENSP00000352154.5:p.Pro24375His
|
|
ENST00000460472.6:c.72749C>A
(TTN)
|
ENSP00000434586.1:p.Pro24250His
|
|
ENST00000589042.5:c.99944C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Pro33315His
|
|
ENST00000591111.5:c.95021C>A
(TTN)
|
ENSP00000465570.1:p.Pro31674His
|
|
ENST00000615779.4:c.95021C>A
(TTN)
|
ENSP00000483597.1:p.Pro31674His
|
|
NM_001256850.1:c.95021C>A
(TTN)
|
NP_001243779.1:p.Pro31674His
|
|
NM_001267550.2:c.99944C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Pro33315His
|
|
NM_003319.4:c.72749C>A
(TTN)
|
NP_003310.4:p.Pro24250His
|
|
NM_133378.4:c.92240C>A
(TTN)
|
NP_596869.4:p.Pro30747His
|
|
NM_133432.3:c.73124C>A
(TTN)
|
NP_597676.3:p.Pro24375His
|
|
NM_133437.4:c.73325C>A
(TTN)
|
NP_597681.4:p.Pro24442His
|
|
NR_038271.1:n.446+13529G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.317-196G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.99041C>A
(TTN)
|
XP_011510031.1:p.Pro33014His
|
|
XM_011511730.1:c.72935C>A
(TTN)
|
XP_011510032.1:p.Pro24312His
|
|
XM_011511731.1:c.72794C>A
(TTN)
|
XP_011510033.1:p.Pro24265His
|
|
XM_017004819.1:c.98837C>A
(TTN)
|
XP_016860308.1:p.Pro32946His
|
|
XM_017004820.1:c.94235C>A
(TTN)
|
XP_016860309.1:p.Pro31412His
|
|
XM_017004821.1:c.94232C>A
(TTN)
|
XP_016860310.1:p.Pro31411His
|
|
XM_017004822.1:c.91274C>A
(TTN)
|
XP_016860311.1:p.Pro30425His
|
|
XM_017004823.1:c.72890C>A
(TTN)
|
XP_016860312.1:p.Pro24297His
|
|
XM_024453094.1:c.94385C>A
(TTN)
|
XP_024308862.1:p.Pro31462His
|
|
XM_024453095.1:c.94382C>A
(TTN)
|
XP_024308863.1:p.Pro31461His
|
|
XM_024453096.1:c.93815C>A
(TTN)
|
XP_024308864.1:p.Pro31272His
|
|
XM_024453097.1:c.91157C>A
(TTN)
|
XP_024308865.1:p.Pro30386His
|
|
XM_024453098.1:c.91076C>A
(TTN)
|
XP_024308866.1:p.Pro30359His
|
|
XM_024453099.1:c.72839C>A
(TTN)
|
XP_024308867.1:p.Pro24280His
|
|
XM_024453100.1:c.62693C>A
(TTN)
|
XP_024308868.1:p.Pro20898His
|
|