ENST00000342992.11:c.100147G>C
(TTN)
|
ENSP00000343764.6:p.Asp33383His
|
|
ENST00000342175.11:c.81232G>C
(TTN)
|
ENSP00000340554.6:p.Asp27078His
|
|
ENST00000359218.10:c.81031G>C
(TTN)
|
ENSP00000352154.5:p.Asp27011His
|
|
ENST00000342175.10:c.81232G>C
(TTN)
|
ENSP00000340554.6:p.Asp27078His
|
|
ENST00000342992.10:c.100147G>C
(TTN)
|
ENSP00000343764.6:p.Asp33383His
|
|
ENST00000359218.9:c.81031G>C
(TTN)
|
ENSP00000352154.5:p.Asp27011His
|
|
ENST00000460472.6:c.80656G>C
(TTN)
|
ENSP00000434586.1:p.Asp26886His
|
|
ENST00000589042.5:c.107851G>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp35951His
|
|
ENST00000591111.5:c.102928G>C
(TTN)
|
ENSP00000465570.1:p.Asp34310His
|
|
ENST00000615779.4:c.102928G>C
(TTN)
|
ENSP00000483597.1:p.Asp34310His
|
|
NM_001256850.1:c.102928G>C
(TTN)
|
NP_001243779.1:p.Asp34310His
|
|
NM_001267550.2:c.107851G>C
(TTN)
MANE Select
|
NP_001254479.2:p.Asp35951His
|
|
NM_003319.4:c.80656G>C
(TTN)
|
NP_003310.4:p.Asp26886His
|
|
NM_133378.4:c.100147G>C
(TTN)
|
NP_596869.4:p.Asp33383His
|
|
NM_133432.3:c.81031G>C
(TTN)
|
NP_597676.3:p.Asp27011His
|
|
NM_133437.4:c.81232G>C
(TTN)
|
NP_597681.4:p.Asp27078His
|
|
NR_038271.1:n.446+3501C>G
(TTN-AS1)
|
|
|
NR_038272.1:n.219+3501C>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.106948G>C
(TTN)
|
XP_011510031.1:p.Asp35650His
|
|
XM_011511730.1:c.80842G>C
(TTN)
|
XP_011510032.1:p.Asp26948His
|
|
XM_011511731.1:c.80701G>C
(TTN)
|
XP_011510033.1:p.Asp26901His
|
|
XM_017004819.1:c.106744G>C
(TTN)
|
XP_016860308.1:p.Asp35582His
|
|
XM_017004820.1:c.102142G>C
(TTN)
|
XP_016860309.1:p.Asp34048His
|
|
XM_017004821.1:c.102139G>C
(TTN)
|
XP_016860310.1:p.Asp34047His
|
|
XM_017004822.1:c.99181G>C
(TTN)
|
XP_016860311.1:p.Asp33061His
|
|
XM_017004823.1:c.80797G>C
(TTN)
|
XP_016860312.1:p.Asp26933His
|
|
XM_024453094.1:c.102292G>C
(TTN)
|
XP_024308862.1:p.Asp34098His
|
|
XM_024453095.1:c.102289G>C
(TTN)
|
XP_024308863.1:p.Asp34097His
|
|
XM_024453096.1:c.101722G>C
(TTN)
|
XP_024308864.1:p.Asp33908His
|
|
XM_024453097.1:c.99064G>C
(TTN)
|
XP_024308865.1:p.Asp33022His
|
|
XM_024453098.1:c.98983G>C
(TTN)
|
XP_024308866.1:p.Asp32995His
|
|
XM_024453099.1:c.80746G>C
(TTN)
|
XP_024308867.1:p.Asp26916His
|
|
XM_024453100.1:c.70600G>C
(TTN)
|
XP_024308868.1:p.Asp23534His
|
|