ENST00000342992.11:c.52996C>T
(TTN)
|
ENSP00000343764.6:p.Pro17666Ser
|
|
ENST00000342175.11:c.34081C>T
(TTN)
|
ENSP00000340554.6:p.Pro11361Ser
|
|
ENST00000359218.10:c.33880C>T
(TTN)
|
ENSP00000352154.5:p.Pro11294Ser
|
|
ENST00000342175.10:c.34081C>T
(TTN)
|
ENSP00000340554.6:p.Pro11361Ser
|
|
ENST00000342992.10:c.52996C>T
(TTN)
|
ENSP00000343764.6:p.Pro17666Ser
|
|
ENST00000359218.9:c.33880C>T
(TTN)
|
ENSP00000352154.5:p.Pro11294Ser
|
|
ENST00000460472.6:c.33505C>T
(TTN)
|
ENSP00000434586.1:p.Pro11169Ser
|
|
ENST00000589042.5:c.60700C>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Pro20234Ser
|
|
ENST00000591111.5:c.55777C>T
(TTN)
|
ENSP00000465570.1:p.Pro18593Ser
|
|
ENST00000615779.4:c.55777C>T
(TTN)
|
ENSP00000483597.1:p.Pro18593Ser
|
|
NM_001256850.1:c.55777C>T
(TTN)
|
NP_001243779.1:p.Pro18593Ser
|
|
NM_001267550.2:c.60700C>T
(TTN)
MANE Select
|
NP_001254479.2:p.Pro20234Ser
|
|
NM_003319.4:c.33505C>T
(TTN)
|
NP_003310.4:p.Pro11169Ser
|
|
NM_133378.4:c.52996C>T
(TTN)
|
NP_596869.4:p.Pro17666Ser
|
|
NM_133432.3:c.33880C>T
(TTN)
|
NP_597676.3:p.Pro11294Ser
|
|
NM_133437.4:c.34081C>T
(TTN)
|
NP_597681.4:p.Pro11361Ser
|
|
NR_038271.1:n.597-6571G>A
(TTN-AS1)
|
|
|
NR_038272.1:n.3189-114G>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.59797C>T
(TTN)
|
XP_011510031.1:p.Pro19933Ser
|
|
XM_011511730.1:c.33691C>T
(TTN)
|
XP_011510032.1:p.Pro11231Ser
|
|
XM_011511731.1:c.33550C>T
(TTN)
|
XP_011510033.1:p.Pro11184Ser
|
|
XM_017004819.1:c.59593C>T
(TTN)
|
XP_016860308.1:p.Pro19865Ser
|
|
XM_017004820.1:c.54991C>T
(TTN)
|
XP_016860309.1:p.Pro18331Ser
|
|
XM_017004821.1:c.54988C>T
(TTN)
|
XP_016860310.1:p.Pro18330Ser
|
|
XM_017004822.1:c.52030C>T
(TTN)
|
XP_016860311.1:p.Pro17344Ser
|
|
XM_017004823.1:c.33646C>T
(TTN)
|
XP_016860312.1:p.Pro11216Ser
|
|
XM_024453094.1:c.55141C>T
(TTN)
|
XP_024308862.1:p.Pro18381Ser
|
|
XM_024453095.1:c.55138C>T
(TTN)
|
XP_024308863.1:p.Pro18380Ser
|
|
XM_024453096.1:c.54571C>T
(TTN)
|
XP_024308864.1:p.Pro18191Ser
|
|
XM_024453097.1:c.51913C>T
(TTN)
|
XP_024308865.1:p.Pro17305Ser
|
|
XM_024453098.1:c.51832C>T
(TTN)
|
XP_024308866.1:p.Pro17278Ser
|
|
XM_024453099.1:c.33595C>T
(TTN)
|
XP_024308867.1:p.Pro11199Ser
|
|
XM_024453100.1:c.23449C>T
(TTN)
|
XP_024308868.1:p.Pro7817Ser
|
|