ENST00000342992.11:c.98343C>G
(TTN)
|
ENSP00000343764.6:p.Leu32781=
|
|
ENST00000342175.11:c.79428C>G
(TTN)
|
ENSP00000340554.6:p.Leu26476=
|
|
ENST00000359218.10:c.79227C>G
(TTN)
|
ENSP00000352154.5:p.Leu26409=
|
|
ENST00000342175.10:c.79428C>G
(TTN)
|
ENSP00000340554.6:p.Leu26476=
|
|
ENST00000342992.10:c.98343C>G
(TTN)
|
ENSP00000343764.6:p.Leu32781=
|
|
ENST00000359218.9:c.79227C>G
(TTN)
|
ENSP00000352154.5:p.Leu26409=
|
|
ENST00000460472.6:c.78852C>G
(TTN)
|
ENSP00000434586.1:p.Leu26284=
|
|
ENST00000589042.5:c.106047C>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu35349=
|
|
ENST00000591111.5:c.101124C>G
(TTN)
|
ENSP00000465570.1:p.Leu33708=
|
|
ENST00000615779.4:c.101124C>G
(TTN)
|
ENSP00000483597.1:p.Leu33708=
|
|
NM_001256850.1:c.101124C>G
(TTN)
|
NP_001243779.1:p.Leu33708=
|
|
NM_001267550.2:c.106047C>G
(TTN)
MANE Select
|
NP_001254479.2:p.Leu35349=
|
|
NM_003319.4:c.78852C>G
(TTN)
|
NP_003310.4:p.Leu26284=
|
|
NM_133378.4:c.98343C>G
(TTN)
|
NP_596869.4:p.Leu32781=
|
|
NM_133432.3:c.79227C>G
(TTN)
|
NP_597676.3:p.Leu26409=
|
|
NM_133437.4:c.79428C>G
(TTN)
|
NP_597681.4:p.Leu26476=
|
|
NR_038271.1:n.446+6932G>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5164G>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.105144C>G
(TTN)
|
XP_011510031.1:p.Leu35048=
|
|
XM_011511730.1:c.79038C>G
(TTN)
|
XP_011510032.1:p.Leu26346=
|
|
XM_011511731.1:c.78897C>G
(TTN)
|
XP_011510033.1:p.Leu26299=
|
|
XM_017004819.1:c.104940C>G
(TTN)
|
XP_016860308.1:p.Leu34980=
|
|
XM_017004820.1:c.100338C>G
(TTN)
|
XP_016860309.1:p.Leu33446=
|
|
XM_017004821.1:c.100335C>G
(TTN)
|
XP_016860310.1:p.Leu33445=
|
|
XM_017004822.1:c.97377C>G
(TTN)
|
XP_016860311.1:p.Leu32459=
|
|
XM_017004823.1:c.78993C>G
(TTN)
|
XP_016860312.1:p.Leu26331=
|
|
XM_024453094.1:c.100488C>G
(TTN)
|
XP_024308862.1:p.Leu33496=
|
|
XM_024453095.1:c.100485C>G
(TTN)
|
XP_024308863.1:p.Leu33495=
|
|
XM_024453096.1:c.99918C>G
(TTN)
|
XP_024308864.1:p.Leu33306=
|
|
XM_024453097.1:c.97260C>G
(TTN)
|
XP_024308865.1:p.Leu32420=
|
|
XM_024453098.1:c.97179C>G
(TTN)
|
XP_024308866.1:p.Leu32393=
|
|
XM_024453099.1:c.78942C>G
(TTN)
|
XP_024308867.1:p.Leu26314=
|
|
XM_024453100.1:c.68796C>G
(TTN)
|
XP_024308868.1:p.Leu22932=
|
|