ENST00000342992.11:c.52215T>C
(TTN)
|
ENSP00000343764.6:p.Asp17405=
|
|
ENST00000342175.11:c.33300T>C
(TTN)
|
ENSP00000340554.6:p.Asp11100=
|
|
ENST00000359218.10:c.33099T>C
(TTN)
|
ENSP00000352154.5:p.Asp11033=
|
|
ENST00000342175.10:c.33300T>C
(TTN)
|
ENSP00000340554.6:p.Asp11100=
|
|
ENST00000342992.10:c.52215T>C
(TTN)
|
ENSP00000343764.6:p.Asp17405=
|
|
ENST00000359218.9:c.33099T>C
(TTN)
|
ENSP00000352154.5:p.Asp11033=
|
|
ENST00000460472.6:c.32724T>C
(TTN)
|
ENSP00000434586.1:p.Asp10908=
|
|
ENST00000589042.5:c.59919T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp19973=
|
|
ENST00000591111.5:c.54996T>C
(TTN)
|
ENSP00000465570.1:p.Asp18332=
|
|
ENST00000615779.4:c.54996T>C
(TTN)
|
ENSP00000483597.1:p.Asp18332=
|
|
NM_001256850.1:c.54996T>C
(TTN)
|
NP_001243779.1:p.Asp18332=
|
|
NM_001267550.2:c.59919T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Asp19973=
|
|
NM_003319.4:c.32724T>C
(TTN)
|
NP_003310.4:p.Asp10908=
|
|
NM_133378.4:c.52215T>C
(TTN)
|
NP_596869.4:p.Asp17405=
|
|
NM_133432.3:c.33099T>C
(TTN)
|
NP_597676.3:p.Asp11033=
|
|
NM_133437.4:c.33300T>C
(TTN)
|
NP_597681.4:p.Asp11100=
|
|
NR_038271.1:n.597-5611A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.3364+671A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.59016T>C
(TTN)
|
XP_011510031.1:p.Asp19672=
|
|
XM_011511730.1:c.32910T>C
(TTN)
|
XP_011510032.1:p.Asp10970=
|
|
XM_011511731.1:c.32769T>C
(TTN)
|
XP_011510033.1:p.Asp10923=
|
|
XM_017004819.1:c.58812T>C
(TTN)
|
XP_016860308.1:p.Asp19604=
|
|
XM_017004820.1:c.54210T>C
(TTN)
|
XP_016860309.1:p.Asp18070=
|
|
XM_017004821.1:c.54207T>C
(TTN)
|
XP_016860310.1:p.Asp18069=
|
|
XM_017004822.1:c.51249T>C
(TTN)
|
XP_016860311.1:p.Asp17083=
|
|
XM_017004823.1:c.32865T>C
(TTN)
|
XP_016860312.1:p.Asp10955=
|
|
XM_024453094.1:c.54360T>C
(TTN)
|
XP_024308862.1:p.Asp18120=
|
|
XM_024453095.1:c.54357T>C
(TTN)
|
XP_024308863.1:p.Asp18119=
|
|
XM_024453096.1:c.53790T>C
(TTN)
|
XP_024308864.1:p.Asp17930=
|
|
XM_024453097.1:c.51132T>C
(TTN)
|
XP_024308865.1:p.Asp17044=
|
|
XM_024453098.1:c.51051T>C
(TTN)
|
XP_024308866.1:p.Asp17017=
|
|
XM_024453099.1:c.32814T>C
(TTN)
|
XP_024308867.1:p.Asp10938=
|
|
XM_024453100.1:c.22668T>C
(TTN)
|
XP_024308868.1:p.Asp7556=
|
|