ENST00000342992.11:c.45302C>A
(TTN)
|
ENSP00000343764.6:p.Pro15101His
|
|
ENST00000342175.11:c.26387C>A
(TTN)
|
ENSP00000340554.6:p.Pro8796His
|
|
ENST00000359218.10:c.26186C>A
(TTN)
|
ENSP00000352154.5:p.Pro8729His
|
|
ENST00000342175.10:c.26387C>A
(TTN)
|
ENSP00000340554.6:p.Pro8796His
|
|
ENST00000342992.10:c.45302C>A
(TTN)
|
ENSP00000343764.6:p.Pro15101His
|
|
ENST00000359218.9:c.26186C>A
(TTN)
|
ENSP00000352154.5:p.Pro8729His
|
|
ENST00000460472.6:c.25811C>A
(TTN)
|
ENSP00000434586.1:p.Pro8604His
|
|
ENST00000589042.5:c.53006C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Pro17669His
|
|
ENST00000591111.5:c.48083C>A
(TTN)
|
ENSP00000465570.1:p.Pro16028His
|
|
ENST00000615779.4:c.48083C>A
(TTN)
|
ENSP00000483597.1:p.Pro16028His
|
|
NM_001256850.1:c.48083C>A
(TTN)
|
NP_001243779.1:p.Pro16028His
|
|
NM_001267550.2:c.53006C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Pro17669His
|
|
NM_003319.4:c.25811C>A
(TTN)
|
NP_003310.4:p.Pro8604His
|
|
NM_133378.4:c.45302C>A
(TTN)
|
NP_596869.4:p.Pro15101His
|
|
NM_133432.3:c.26186C>A
(TTN)
|
NP_597676.3:p.Pro8729His
|
|
NM_133437.4:c.26387C>A
(TTN)
|
NP_597681.4:p.Pro8796His
|
|
NR_038271.1:n.683-485G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.52103C>A
(TTN)
|
XP_011510031.1:p.Pro17368His
|
|
XM_011511730.1:c.25997C>A
(TTN)
|
XP_011510032.1:p.Pro8666His
|
|
XM_011511731.1:c.25856C>A
(TTN)
|
XP_011510033.1:p.Pro8619His
|
|
XM_017004819.1:c.51899C>A
(TTN)
|
XP_016860308.1:p.Pro17300His
|
|
XM_017004820.1:c.47297C>A
(TTN)
|
XP_016860309.1:p.Pro15766His
|
|
XM_017004821.1:c.47294C>A
(TTN)
|
XP_016860310.1:p.Pro15765His
|
|
XM_017004822.1:c.44336C>A
(TTN)
|
XP_016860311.1:p.Pro14779His
|
|
XM_017004823.1:c.25952C>A
(TTN)
|
XP_016860312.1:p.Pro8651His
|
|
XM_024453094.1:c.47447C>A
(TTN)
|
XP_024308862.1:p.Pro15816His
|
|
XM_024453095.1:c.47444C>A
(TTN)
|
XP_024308863.1:p.Pro15815His
|
|
XM_024453096.1:c.46877C>A
(TTN)
|
XP_024308864.1:p.Pro15626His
|
|
XM_024453097.1:c.44219C>A
(TTN)
|
XP_024308865.1:p.Pro14740His
|
|
XM_024453098.1:c.44138C>A
(TTN)
|
XP_024308866.1:p.Pro14713His
|
|
XM_024453099.1:c.25901C>A
(TTN)
|
XP_024308867.1:p.Pro8634His
|
|
XM_024453100.1:c.15755C>A
(TTN)
|
XP_024308868.1:p.Pro5252His
|
|