ENST00000342992.11:c.88959T>C
(TTN)
|
ENSP00000343764.6:p.Leu29653=
|
|
ENST00000342175.11:c.70044T>C
(TTN)
|
ENSP00000340554.6:p.Leu23348=
|
|
ENST00000359218.10:c.69843T>C
(TTN)
|
ENSP00000352154.5:p.Leu23281=
|
|
ENST00000342175.10:c.70044T>C
(TTN)
|
ENSP00000340554.6:p.Leu23348=
|
|
ENST00000342992.10:c.88959T>C
(TTN)
|
ENSP00000343764.6:p.Leu29653=
|
|
ENST00000359218.9:c.69843T>C
(TTN)
|
ENSP00000352154.5:p.Leu23281=
|
|
ENST00000460472.6:c.69468T>C
(TTN)
|
ENSP00000434586.1:p.Leu23156=
|
|
ENST00000589042.5:c.96663T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu32221=
|
|
ENST00000591111.5:c.91740T>C
(TTN)
|
ENSP00000465570.1:p.Leu30580=
|
|
ENST00000615779.4:c.91740T>C
(TTN)
|
ENSP00000483597.1:p.Leu30580=
|
|
NM_001256850.1:c.91740T>C
(TTN)
|
NP_001243779.1:p.Leu30580=
|
|
NM_001267550.2:c.96663T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Leu32221=
|
|
NM_003319.4:c.69468T>C
(TTN)
|
NP_003310.4:p.Leu23156=
|
|
NM_133378.4:c.88959T>C
(TTN)
|
NP_596869.4:p.Leu29653=
|
|
NM_133432.3:c.69843T>C
(TTN)
|
NP_597676.3:p.Leu23281=
|
|
NM_133437.4:c.70044T>C
(TTN)
|
NP_597681.4:p.Leu23348=
|
|
NR_038271.1:n.446+19674A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+949A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.95760T>C
(TTN)
|
XP_011510031.1:p.Leu31920=
|
|
XM_011511730.1:c.69654T>C
(TTN)
|
XP_011510032.1:p.Leu23218=
|
|
XM_011511731.1:c.69513T>C
(TTN)
|
XP_011510033.1:p.Leu23171=
|
|
XM_017004819.1:c.95556T>C
(TTN)
|
XP_016860308.1:p.Leu31852=
|
|
XM_017004820.1:c.90954T>C
(TTN)
|
XP_016860309.1:p.Leu30318=
|
|
XM_017004821.1:c.90951T>C
(TTN)
|
XP_016860310.1:p.Leu30317=
|
|
XM_017004822.1:c.87993T>C
(TTN)
|
XP_016860311.1:p.Leu29331=
|
|
XM_017004823.1:c.69609T>C
(TTN)
|
XP_016860312.1:p.Leu23203=
|
|
XM_024453094.1:c.91104T>C
(TTN)
|
XP_024308862.1:p.Leu30368=
|
|
XM_024453095.1:c.91101T>C
(TTN)
|
XP_024308863.1:p.Leu30367=
|
|
XM_024453096.1:c.90534T>C
(TTN)
|
XP_024308864.1:p.Leu30178=
|
|
XM_024453097.1:c.87876T>C
(TTN)
|
XP_024308865.1:p.Leu29292=
|
|
XM_024453098.1:c.87795T>C
(TTN)
|
XP_024308866.1:p.Leu29265=
|
|
XM_024453099.1:c.69558T>C
(TTN)
|
XP_024308867.1:p.Leu23186=
|
|
XM_024453100.1:c.59412T>C
(TTN)
|
XP_024308868.1:p.Leu19804=
|
|