|
NM_001267550.2:c.66726C>T
(TTN)
MANE Select
|
NP_001254479.2:p.Asp22242=
|
|
ENST00000589042.5:c.66726C>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp22242=
|
|
NM_001256850.1:c.61803C>T
(TTN)
|
NP_001243779.1:p.Asp20601=
|
|
NM_003319.4:c.39531C>T
(TTN)
|
NP_003310.4:p.Asp13177=
|
|
NM_133378.4:c.59022C>T
(TTN)
|
NP_596869.4:p.Asp19674=
|
|
NM_133432.3:c.39906C>T
(TTN)
|
NP_597676.3:p.Asp13302=
|
|
NM_133437.4:c.40107C>T
(TTN)
|
NP_597681.4:p.Asp13369=
|
|
NR_038271.1:n.596+10093G>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-1030G>A
(TTN-AS1)
|
|
|
ENST00000342175.10:c.40107C>T
(TTN)
|
ENSP00000340554.6:p.Asp13369=
|
|
ENST00000342175.11:c.40107C>T
(TTN)
|
ENSP00000340554.6:p.Asp13369=
|
|
ENST00000342992.10:c.59022C>T
(TTN)
|
ENSP00000343764.6:p.Asp19674=
|
|
ENST00000342992.11:c.59022C>T
(TTN)
|
ENSP00000343764.6:p.Asp19674=
|
|
ENST00000359218.10:c.39906C>T
(TTN)
|
ENSP00000352154.5:p.Asp13302=
|
|
ENST00000359218.9:c.39906C>T
(TTN)
|
ENSP00000352154.5:p.Asp13302=
|
|
ENST00000460472.6:c.39531C>T
(TTN)
|
ENSP00000434586.1:p.Asp13177=
|
|
ENST00000591111.5:c.61803C>T
(TTN)
|
ENSP00000465570.1:p.Asp20601=
|
|
ENST00000615779.4:c.61803C>T
(TTN)
|
ENSP00000483597.1:p.Asp20601=
|
|
XM_011511729.1:c.65823C>T
(TTN)
|
XP_011510031.1:p.Asp21941=
|
|
XM_011511730.1:c.39717C>T
(TTN)
|
XP_011510032.1:p.Asp13239=
|
|
XM_011511731.1:c.39576C>T
(TTN)
|
XP_011510033.1:p.Asp13192=
|
|
XM_017004819.1:c.65619C>T
(TTN)
|
XP_016860308.1:p.Asp21873=
|
|
XM_017004820.1:c.61017C>T
(TTN)
|
XP_016860309.1:p.Asp20339=
|
|
XM_017004821.1:c.61014C>T
(TTN)
|
XP_016860310.1:p.Asp20338=
|
|
XM_017004822.1:c.58056C>T
(TTN)
|
XP_016860311.1:p.Asp19352=
|
|
XM_017004823.1:c.39672C>T
(TTN)
|
XP_016860312.1:p.Asp13224=
|
|
XM_024453094.1:c.61167C>T
(TTN)
|
XP_024308862.1:p.Asp20389=
|
|
XM_024453095.1:c.61164C>T
(TTN)
|
XP_024308863.1:p.Asp20388=
|
|
XM_024453096.1:c.60597C>T
(TTN)
|
XP_024308864.1:p.Asp20199=
|
|
XM_024453097.1:c.57939C>T
(TTN)
|
XP_024308865.1:p.Asp19313=
|
|
XM_024453098.1:c.57858C>T
(TTN)
|
XP_024308866.1:p.Asp19286=
|
|
XM_024453099.1:c.39621C>T
(TTN)
|
XP_024308867.1:p.Asp13207=
|
|
XM_024453100.1:c.29475C>T
(TTN)
|
XP_024308868.1:p.Asp9825=
|
