ENST00000342992.11:c.64087C>T
(TTN)
|
ENSP00000343764.6:p.Pro21363Ser
|
|
ENST00000342175.11:c.45172C>T
(TTN)
|
ENSP00000340554.6:p.Pro15058Ser
|
|
ENST00000359218.10:c.44971C>T
(TTN)
|
ENSP00000352154.5:p.Pro14991Ser
|
|
ENST00000342175.10:c.45172C>T
(TTN)
|
ENSP00000340554.6:p.Pro15058Ser
|
|
ENST00000342992.10:c.64087C>T
(TTN)
|
ENSP00000343764.6:p.Pro21363Ser
|
|
ENST00000359218.9:c.44971C>T
(TTN)
|
ENSP00000352154.5:p.Pro14991Ser
|
|
ENST00000460472.6:c.44596C>T
(TTN)
|
ENSP00000434586.1:p.Pro14866Ser
|
|
ENST00000589042.5:c.71791C>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Pro23931Ser
|
|
ENST00000591111.5:c.66868C>T
(TTN)
|
ENSP00000465570.1:p.Pro22290Ser
|
|
ENST00000615779.4:c.66868C>T
(TTN)
|
ENSP00000483597.1:p.Pro22290Ser
|
|
NM_001256850.1:c.66868C>T
(TTN)
|
NP_001243779.1:p.Pro22290Ser
|
|
NM_001267550.2:c.71791C>T
(TTN)
MANE Select
|
NP_001254479.2:p.Pro23931Ser
|
|
NM_003319.4:c.44596C>T
(TTN)
|
NP_003310.4:p.Pro14866Ser
|
|
NM_133378.4:c.64087C>T
(TTN)
|
NP_596869.4:p.Pro21363Ser
|
|
NM_133432.3:c.44971C>T
(TTN)
|
NP_597676.3:p.Pro14991Ser
|
|
NM_133437.4:c.45172C>T
(TTN)
|
NP_597681.4:p.Pro15058Ser
|
|
NR_038271.1:n.596+2892G>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-8231G>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.70888C>T
(TTN)
|
XP_011510031.1:p.Pro23630Ser
|
|
XM_011511730.1:c.44782C>T
(TTN)
|
XP_011510032.1:p.Pro14928Ser
|
|
XM_011511731.1:c.44641C>T
(TTN)
|
XP_011510033.1:p.Pro14881Ser
|
|
XM_017004819.1:c.70684C>T
(TTN)
|
XP_016860308.1:p.Pro23562Ser
|
|
XM_017004820.1:c.66082C>T
(TTN)
|
XP_016860309.1:p.Pro22028Ser
|
|
XM_017004821.1:c.66079C>T
(TTN)
|
XP_016860310.1:p.Pro22027Ser
|
|
XM_017004822.1:c.63121C>T
(TTN)
|
XP_016860311.1:p.Pro21041Ser
|
|
XM_017004823.1:c.44737C>T
(TTN)
|
XP_016860312.1:p.Pro14913Ser
|
|
XM_024453094.1:c.66232C>T
(TTN)
|
XP_024308862.1:p.Pro22078Ser
|
|
XM_024453095.1:c.66229C>T
(TTN)
|
XP_024308863.1:p.Pro22077Ser
|
|
XM_024453096.1:c.65662C>T
(TTN)
|
XP_024308864.1:p.Pro21888Ser
|
|
XM_024453097.1:c.63004C>T
(TTN)
|
XP_024308865.1:p.Pro21002Ser
|
|
XM_024453098.1:c.62923C>T
(TTN)
|
XP_024308866.1:p.Pro20975Ser
|
|
XM_024453099.1:c.44686C>T
(TTN)
|
XP_024308867.1:p.Pro14896Ser
|
|
XM_024453100.1:c.34540C>T
(TTN)
|
XP_024308868.1:p.Pro11514Ser
|
|