ENST00000342992.11:c.57273T>G
(TTN)
|
ENSP00000343764.6:p.Val19091=
|
|
ENST00000342175.11:c.38358T>G
(TTN)
|
ENSP00000340554.6:p.Val12786=
|
|
ENST00000359218.10:c.38157T>G
(TTN)
|
ENSP00000352154.5:p.Val12719=
|
|
ENST00000342175.10:c.38358T>G
(TTN)
|
ENSP00000340554.6:p.Val12786=
|
|
ENST00000342992.10:c.57273T>G
(TTN)
|
ENSP00000343764.6:p.Val19091=
|
|
ENST00000359218.9:c.38157T>G
(TTN)
|
ENSP00000352154.5:p.Val12719=
|
|
ENST00000460472.6:c.37782T>G
(TTN)
|
ENSP00000434586.1:p.Val12594=
|
|
ENST00000589042.5:c.64977T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Val21659=
|
|
ENST00000591111.5:c.60054T>G
(TTN)
|
ENSP00000465570.1:p.Val20018=
|
|
ENST00000615779.4:c.60054T>G
(TTN)
|
ENSP00000483597.1:p.Val20018=
|
|
NM_001256850.1:c.60054T>G
(TTN)
|
NP_001243779.1:p.Val20018=
|
|
NM_001267550.2:c.64977T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Val21659=
|
|
NM_003319.4:c.37782T>G
(TTN)
|
NP_003310.4:p.Val12594=
|
|
NM_133378.4:c.57273T>G
(TTN)
|
NP_596869.4:p.Val19091=
|
|
NM_133432.3:c.38157T>G
(TTN)
|
NP_597676.3:p.Val12719=
|
|
NM_133437.4:c.38358T>G
(TTN)
|
NP_597681.4:p.Val12786=
|
|
NR_038271.1:n.597-13022A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2769A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.64074T>G
(TTN)
|
XP_011510031.1:p.Val21358=
|
|
XM_011511730.1:c.37968T>G
(TTN)
|
XP_011510032.1:p.Val12656=
|
|
XM_011511731.1:c.37827T>G
(TTN)
|
XP_011510033.1:p.Val12609=
|
|
XM_017004819.1:c.63870T>G
(TTN)
|
XP_016860308.1:p.Val21290=
|
|
XM_017004820.1:c.59268T>G
(TTN)
|
XP_016860309.1:p.Val19756=
|
|
XM_017004821.1:c.59265T>G
(TTN)
|
XP_016860310.1:p.Val19755=
|
|
XM_017004822.1:c.56307T>G
(TTN)
|
XP_016860311.1:p.Val18769=
|
|
XM_017004823.1:c.37923T>G
(TTN)
|
XP_016860312.1:p.Val12641=
|
|
XM_024453094.1:c.59418T>G
(TTN)
|
XP_024308862.1:p.Val19806=
|
|
XM_024453095.1:c.59415T>G
(TTN)
|
XP_024308863.1:p.Val19805=
|
|
XM_024453096.1:c.58848T>G
(TTN)
|
XP_024308864.1:p.Val19616=
|
|
XM_024453097.1:c.56190T>G
(TTN)
|
XP_024308865.1:p.Val18730=
|
|
XM_024453098.1:c.56109T>G
(TTN)
|
XP_024308866.1:p.Val18703=
|
|
XM_024453099.1:c.37872T>G
(TTN)
|
XP_024308867.1:p.Val12624=
|
|
XM_024453100.1:c.27726T>G
(TTN)
|
XP_024308868.1:p.Val9242=
|
|