ENST00000342992.11:c.83343T>G
(TTN)
|
ENSP00000343764.6:p.Val27781=
|
|
ENST00000342175.11:c.64428T>G
(TTN)
|
ENSP00000340554.6:p.Val21476=
|
|
ENST00000359218.10:c.64227T>G
(TTN)
|
ENSP00000352154.5:p.Val21409=
|
|
ENST00000342175.10:c.64428T>G
(TTN)
|
ENSP00000340554.6:p.Val21476=
|
|
ENST00000342992.10:c.83343T>G
(TTN)
|
ENSP00000343764.6:p.Val27781=
|
|
ENST00000359218.9:c.64227T>G
(TTN)
|
ENSP00000352154.5:p.Val21409=
|
|
ENST00000460472.6:c.63852T>G
(TTN)
|
ENSP00000434586.1:p.Val21284=
|
|
ENST00000589042.5:c.91047T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Val30349=
|
|
ENST00000591111.5:c.86124T>G
(TTN)
|
ENSP00000465570.1:p.Val28708=
|
|
ENST00000615779.4:c.86124T>G
(TTN)
|
ENSP00000483597.1:p.Val28708=
|
|
NM_001256850.1:c.86124T>G
(TTN)
|
NP_001243779.1:p.Val28708=
|
|
NM_001267550.2:c.91047T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Val30349=
|
|
NM_003319.4:c.63852T>G
(TTN)
|
NP_003310.4:p.Val21284=
|
|
NM_133378.4:c.83343T>G
(TTN)
|
NP_596869.4:p.Val27781=
|
|
NM_133432.3:c.64227T>G
(TTN)
|
NP_597676.3:p.Val21409=
|
|
NM_133437.4:c.64428T>G
(TTN)
|
NP_597681.4:p.Val21476=
|
|
NR_038271.1:n.447-19447A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+9492A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.90144T>G
(TTN)
|
XP_011510031.1:p.Val30048=
|
|
XM_011511730.1:c.64038T>G
(TTN)
|
XP_011510032.1:p.Val21346=
|
|
XM_011511731.1:c.63897T>G
(TTN)
|
XP_011510033.1:p.Val21299=
|
|
XM_017004819.1:c.89940T>G
(TTN)
|
XP_016860308.1:p.Val29980=
|
|
XM_017004820.1:c.85338T>G
(TTN)
|
XP_016860309.1:p.Val28446=
|
|
XM_017004821.1:c.85335T>G
(TTN)
|
XP_016860310.1:p.Val28445=
|
|
XM_017004822.1:c.82377T>G
(TTN)
|
XP_016860311.1:p.Val27459=
|
|
XM_017004823.1:c.63993T>G
(TTN)
|
XP_016860312.1:p.Val21331=
|
|
XM_024453094.1:c.85488T>G
(TTN)
|
XP_024308862.1:p.Val28496=
|
|
XM_024453095.1:c.85485T>G
(TTN)
|
XP_024308863.1:p.Val28495=
|
|
XM_024453096.1:c.84918T>G
(TTN)
|
XP_024308864.1:p.Val28306=
|
|
XM_024453097.1:c.82260T>G
(TTN)
|
XP_024308865.1:p.Val27420=
|
|
XM_024453098.1:c.82179T>G
(TTN)
|
XP_024308866.1:p.Val27393=
|
|
XM_024453099.1:c.63942T>G
(TTN)
|
XP_024308867.1:p.Val21314=
|
|
XM_024453100.1:c.53796T>G
(TTN)
|
XP_024308868.1:p.Val17932=
|
|