ENST00000342992.11:c.52217C>G
(TTN)
|
ENSP00000343764.6:p.Pro17406Arg
|
|
ENST00000342175.11:c.33302C>G
(TTN)
|
ENSP00000340554.6:p.Pro11101Arg
|
|
ENST00000359218.10:c.33101C>G
(TTN)
|
ENSP00000352154.5:p.Pro11034Arg
|
|
ENST00000342175.10:c.33302C>G
(TTN)
|
ENSP00000340554.6:p.Pro11101Arg
|
|
ENST00000342992.10:c.52217C>G
(TTN)
|
ENSP00000343764.6:p.Pro17406Arg
|
|
ENST00000359218.9:c.33101C>G
(TTN)
|
ENSP00000352154.5:p.Pro11034Arg
|
|
ENST00000460472.6:c.32726C>G
(TTN)
|
ENSP00000434586.1:p.Pro10909Arg
|
|
ENST00000589042.5:c.59921C>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Pro19974Arg
|
|
ENST00000591111.5:c.54998C>G
(TTN)
|
ENSP00000465570.1:p.Pro18333Arg
|
|
ENST00000615779.4:c.54998C>G
(TTN)
|
ENSP00000483597.1:p.Pro18333Arg
|
|
NM_001256850.1:c.54998C>G
(TTN)
|
NP_001243779.1:p.Pro18333Arg
|
|
NM_001267550.2:c.59921C>G
(TTN)
MANE Select
|
NP_001254479.2:p.Pro19974Arg
|
|
NM_003319.4:c.32726C>G
(TTN)
|
NP_003310.4:p.Pro10909Arg
|
|
NM_133378.4:c.52217C>G
(TTN)
|
NP_596869.4:p.Pro17406Arg
|
|
NM_133432.3:c.33101C>G
(TTN)
|
NP_597676.3:p.Pro11034Arg
|
|
NM_133437.4:c.33302C>G
(TTN)
|
NP_597681.4:p.Pro11101Arg
|
|
NR_038271.1:n.597-5613G>C
(TTN-AS1)
|
|
|
NR_038272.1:n.3364+669G>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.59018C>G
(TTN)
|
XP_011510031.1:p.Pro19673Arg
|
|
XM_011511730.1:c.32912C>G
(TTN)
|
XP_011510032.1:p.Pro10971Arg
|
|
XM_011511731.1:c.32771C>G
(TTN)
|
XP_011510033.1:p.Pro10924Arg
|
|
XM_017004819.1:c.58814C>G
(TTN)
|
XP_016860308.1:p.Pro19605Arg
|
|
XM_017004820.1:c.54212C>G
(TTN)
|
XP_016860309.1:p.Pro18071Arg
|
|
XM_017004821.1:c.54209C>G
(TTN)
|
XP_016860310.1:p.Pro18070Arg
|
|
XM_017004822.1:c.51251C>G
(TTN)
|
XP_016860311.1:p.Pro17084Arg
|
|
XM_017004823.1:c.32867C>G
(TTN)
|
XP_016860312.1:p.Pro10956Arg
|
|
XM_024453094.1:c.54362C>G
(TTN)
|
XP_024308862.1:p.Pro18121Arg
|
|
XM_024453095.1:c.54359C>G
(TTN)
|
XP_024308863.1:p.Pro18120Arg
|
|
XM_024453096.1:c.53792C>G
(TTN)
|
XP_024308864.1:p.Pro17931Arg
|
|
XM_024453097.1:c.51134C>G
(TTN)
|
XP_024308865.1:p.Pro17045Arg
|
|
XM_024453098.1:c.51053C>G
(TTN)
|
XP_024308866.1:p.Pro17018Arg
|
|
XM_024453099.1:c.32816C>G
(TTN)
|
XP_024308867.1:p.Pro10939Arg
|
|
XM_024453100.1:c.22670C>G
(TTN)
|
XP_024308868.1:p.Pro7557Arg
|
|