ENST00000342992.11:c.86855G>T
(TTN)
|
ENSP00000343764.6:p.Arg28952Ile
|
|
ENST00000342175.11:c.67940G>T
(TTN)
|
ENSP00000340554.6:p.Arg22647Ile
|
|
ENST00000359218.10:c.67739G>T
(TTN)
|
ENSP00000352154.5:p.Arg22580Ile
|
|
ENST00000342175.10:c.67940G>T
(TTN)
|
ENSP00000340554.6:p.Arg22647Ile
|
|
ENST00000342992.10:c.86855G>T
(TTN)
|
ENSP00000343764.6:p.Arg28952Ile
|
|
ENST00000359218.9:c.67739G>T
(TTN)
|
ENSP00000352154.5:p.Arg22580Ile
|
|
ENST00000460472.6:c.67364G>T
(TTN)
|
ENSP00000434586.1:p.Arg22455Ile
|
|
ENST00000589042.5:c.94559G>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Arg31520Ile
|
|
ENST00000591111.5:c.89636G>T
(TTN)
|
ENSP00000465570.1:p.Arg29879Ile
|
|
ENST00000615779.4:c.89636G>T
(TTN)
|
ENSP00000483597.1:p.Arg29879Ile
|
|
NM_001256850.1:c.89636G>T
(TTN)
|
NP_001243779.1:p.Arg29879Ile
|
|
NM_001267550.2:c.94559G>T
(TTN)
MANE Select
|
NP_001254479.2:p.Arg31520Ile
|
|
NM_003319.4:c.67364G>T
(TTN)
|
NP_003310.4:p.Arg22455Ile
|
|
NM_133378.4:c.86855G>T
(TTN)
|
NP_596869.4:p.Arg28952Ile
|
|
NM_133432.3:c.67739G>T
(TTN)
|
NP_597676.3:p.Arg22580Ile
|
|
NM_133437.4:c.67940G>T
(TTN)
|
NP_597681.4:p.Arg22647Ile
|
|
NR_038271.1:n.446+23233C>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+4508C>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.93656G>T
(TTN)
|
XP_011510031.1:p.Arg31219Ile
|
|
XM_011511730.1:c.67550G>T
(TTN)
|
XP_011510032.1:p.Arg22517Ile
|
|
XM_011511731.1:c.67409G>T
(TTN)
|
XP_011510033.1:p.Arg22470Ile
|
|
XM_017004819.1:c.93452G>T
(TTN)
|
XP_016860308.1:p.Arg31151Ile
|
|
XM_017004820.1:c.88850G>T
(TTN)
|
XP_016860309.1:p.Arg29617Ile
|
|
XM_017004821.1:c.88847G>T
(TTN)
|
XP_016860310.1:p.Arg29616Ile
|
|
XM_017004822.1:c.85889G>T
(TTN)
|
XP_016860311.1:p.Arg28630Ile
|
|
XM_017004823.1:c.67505G>T
(TTN)
|
XP_016860312.1:p.Arg22502Ile
|
|
XM_024453094.1:c.89000G>T
(TTN)
|
XP_024308862.1:p.Arg29667Ile
|
|
XM_024453095.1:c.88997G>T
(TTN)
|
XP_024308863.1:p.Arg29666Ile
|
|
XM_024453096.1:c.88430G>T
(TTN)
|
XP_024308864.1:p.Arg29477Ile
|
|
XM_024453097.1:c.85772G>T
(TTN)
|
XP_024308865.1:p.Arg28591Ile
|
|
XM_024453098.1:c.85691G>T
(TTN)
|
XP_024308866.1:p.Arg28564Ile
|
|
XM_024453099.1:c.67454G>T
(TTN)
|
XP_024308867.1:p.Arg22485Ile
|
|
XM_024453100.1:c.57308G>T
(TTN)
|
XP_024308868.1:p.Arg19103Ile
|
|