|
ENST00000342992.11:c.90795C>T
(TTN)
|
ENSP00000343764.6:p.Leu30265=
|
|
|
ENST00000342175.11:c.71880C>T
(TTN)
|
ENSP00000340554.6:p.Leu23960=
|
|
|
ENST00000359218.10:c.71679C>T
(TTN)
|
ENSP00000352154.5:p.Leu23893=
|
|
|
ENST00000342175.10:c.71880C>T
(TTN)
|
ENSP00000340554.6:p.Leu23960=
|
|
|
ENST00000342992.10:c.90795C>T
(TTN)
|
ENSP00000343764.6:p.Leu30265=
|
|
|
ENST00000359218.9:c.71679C>T
(TTN)
|
ENSP00000352154.5:p.Leu23893=
|
|
|
ENST00000460472.6:c.71304C>T
(TTN)
|
ENSP00000434586.1:p.Leu23768=
|
|
|
ENST00000589042.5:c.98499C>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu32833=
|
|
|
ENST00000591111.5:c.93576C>T
(TTN)
|
ENSP00000465570.1:p.Leu31192=
|
|
|
ENST00000615779.4:c.93576C>T
(TTN)
|
ENSP00000483597.1:p.Leu31192=
|
|
|
NM_001256850.1:c.93576C>T
(TTN)
|
NP_001243779.1:p.Leu31192=
|
|
|
NM_001267550.2:c.98499C>T
(TTN)
MANE Select
|
NP_001254479.2:p.Leu32833=
|
|
|
NM_003319.4:c.71304C>T
(TTN)
|
NP_003310.4:p.Leu23768=
|
|
|
NM_133378.4:c.90795C>T
(TTN)
|
NP_596869.4:p.Leu30265=
|
|
|
NM_133432.3:c.71679C>T
(TTN)
|
NP_597676.3:p.Leu23893=
|
|
|
NM_133437.4:c.71880C>T
(TTN)
|
NP_597681.4:p.Leu23960=
|
|
|
NR_038271.1:n.446+15930G>A
(TTN-AS1)
|
|
|
|
NR_038272.1:n.1516G>A
(TTN-AS1)
|
|
|
|
XM_011511729.1:c.97596C>T
(TTN)
|
XP_011510031.1:p.Leu32532=
|
|
|
XM_011511730.1:c.71490C>T
(TTN)
|
XP_011510032.1:p.Leu23830=
|
|
|
XM_011511731.1:c.71349C>T
(TTN)
|
XP_011510033.1:p.Leu23783=
|
|
|
XM_017004819.1:c.97392C>T
(TTN)
|
XP_016860308.1:p.Leu32464=
|
|
|
XM_017004820.1:c.92790C>T
(TTN)
|
XP_016860309.1:p.Leu30930=
|
|
|
XM_017004821.1:c.92787C>T
(TTN)
|
XP_016860310.1:p.Leu30929=
|
|
|
XM_017004822.1:c.89829C>T
(TTN)
|
XP_016860311.1:p.Leu29943=
|
|
|
XM_017004823.1:c.71445C>T
(TTN)
|
XP_016860312.1:p.Leu23815=
|
|
|
XM_024453094.1:c.92940C>T
(TTN)
|
XP_024308862.1:p.Leu30980=
|
|
|
XM_024453095.1:c.92937C>T
(TTN)
|
XP_024308863.1:p.Leu30979=
|
|
|
XM_024453096.1:c.92370C>T
(TTN)
|
XP_024308864.1:p.Leu30790=
|
|
|
XM_024453097.1:c.89712C>T
(TTN)
|
XP_024308865.1:p.Leu29904=
|
|
|
XM_024453098.1:c.89631C>T
(TTN)
|
XP_024308866.1:p.Leu29877=
|
|
|
XM_024453099.1:c.71394C>T
(TTN)
|
XP_024308867.1:p.Leu23798=
|
|
|
XM_024453100.1:c.61248C>T
(TTN)
|
XP_024308868.1:p.Leu20416=
|
|
