ENST00000342992.11:c.69001G>C
(TTN)
|
ENSP00000343764.6:p.Asp23001His
|
|
ENST00000342175.11:c.50086G>C
(TTN)
|
ENSP00000340554.6:p.Asp16696His
|
|
ENST00000359218.10:c.49885G>C
(TTN)
|
ENSP00000352154.5:p.Asp16629His
|
|
ENST00000342175.10:c.50086G>C
(TTN)
|
ENSP00000340554.6:p.Asp16696His
|
|
ENST00000342992.10:c.69001G>C
(TTN)
|
ENSP00000343764.6:p.Asp23001His
|
|
ENST00000359218.9:c.49885G>C
(TTN)
|
ENSP00000352154.5:p.Asp16629His
|
|
ENST00000460472.6:c.49510G>C
(TTN)
|
ENSP00000434586.1:p.Asp16504His
|
|
ENST00000589042.5:c.76705G>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp25569His
|
|
ENST00000591111.5:c.71782G>C
(TTN)
|
ENSP00000465570.1:p.Asp23928His
|
|
ENST00000615779.4:c.71782G>C
(TTN)
|
ENSP00000483597.1:p.Asp23928His
|
|
NM_001256850.1:c.71782G>C
(TTN)
|
NP_001243779.1:p.Asp23928His
|
|
NM_001267550.2:c.76705G>C
(TTN)
MANE Select
|
NP_001254479.2:p.Asp25569His
|
|
NM_003319.4:c.49510G>C
(TTN)
|
NP_003310.4:p.Asp16504His
|
|
NM_133378.4:c.69001G>C
(TTN)
|
NP_596869.4:p.Asp23001His
|
|
NM_133432.3:c.49885G>C
(TTN)
|
NP_597676.3:p.Asp16629His
|
|
NM_133437.4:c.50086G>C
(TTN)
|
NP_597681.4:p.Asp16696His
|
|
NR_038271.1:n.447-1873C>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-13145C>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.75802G>C
(TTN)
|
XP_011510031.1:p.Asp25268His
|
|
XM_011511730.1:c.49696G>C
(TTN)
|
XP_011510032.1:p.Asp16566His
|
|
XM_011511731.1:c.49555G>C
(TTN)
|
XP_011510033.1:p.Asp16519His
|
|
XM_017004819.1:c.75598G>C
(TTN)
|
XP_016860308.1:p.Asp25200His
|
|
XM_017004820.1:c.70996G>C
(TTN)
|
XP_016860309.1:p.Asp23666His
|
|
XM_017004821.1:c.70993G>C
(TTN)
|
XP_016860310.1:p.Asp23665His
|
|
XM_017004822.1:c.68035G>C
(TTN)
|
XP_016860311.1:p.Asp22679His
|
|
XM_017004823.1:c.49651G>C
(TTN)
|
XP_016860312.1:p.Asp16551His
|
|
XM_024453094.1:c.71146G>C
(TTN)
|
XP_024308862.1:p.Asp23716His
|
|
XM_024453095.1:c.71143G>C
(TTN)
|
XP_024308863.1:p.Asp23715His
|
|
XM_024453096.1:c.70576G>C
(TTN)
|
XP_024308864.1:p.Asp23526His
|
|
XM_024453097.1:c.67918G>C
(TTN)
|
XP_024308865.1:p.Asp22640His
|
|
XM_024453098.1:c.67837G>C
(TTN)
|
XP_024308866.1:p.Asp22613His
|
|
XM_024453099.1:c.49600G>C
(TTN)
|
XP_024308867.1:p.Asp16534His
|
|
XM_024453100.1:c.39454G>C
(TTN)
|
XP_024308868.1:p.Asp13152His
|
|