ENST00000342992.11:c.39164G>T
(TTN)
|
ENSP00000343764.6:p.Arg13055Ile
|
|
ENST00000342175.11:c.20249G>T
(TTN)
|
ENSP00000340554.6:p.Arg6750Ile
|
|
ENST00000359218.10:c.20048G>T
(TTN)
|
ENSP00000352154.5:p.Arg6683Ile
|
|
ENST00000342175.10:c.20249G>T
(TTN)
|
ENSP00000340554.6:p.Arg6750Ile
|
|
ENST00000342992.10:c.39164G>T
(TTN)
|
ENSP00000343764.6:p.Arg13055Ile
|
|
ENST00000359218.9:c.20048G>T
(TTN)
|
ENSP00000352154.5:p.Arg6683Ile
|
|
ENST00000460472.6:c.19673G>T
(TTN)
|
ENSP00000434586.1:p.Arg6558Ile
|
|
ENST00000589042.5:c.46868G>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Arg15623Ile
|
|
ENST00000591111.5:c.41945G>T
(TTN)
|
ENSP00000465570.1:p.Arg13982Ile
|
|
ENST00000615779.4:c.41945G>T
(TTN)
|
ENSP00000483597.1:p.Arg13982Ile
|
|
NM_001256850.1:c.41945G>T
(TTN)
|
NP_001243779.1:p.Arg13982Ile
|
|
NM_001267550.2:c.46868G>T
(TTN)
MANE Select
|
NP_001254479.2:p.Arg15623Ile
|
|
NM_003319.4:c.19673G>T
(TTN)
|
NP_003310.4:p.Arg6558Ile
|
|
NM_133378.4:c.39164G>T
(TTN)
|
NP_596869.4:p.Arg13055Ile
|
|
NM_133432.3:c.20048G>T
(TTN)
|
NP_597676.3:p.Arg6683Ile
|
|
NM_133437.4:c.20249G>T
(TTN)
|
NP_597681.4:p.Arg6750Ile
|
|
NR_038271.1:n.1605-1071C>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.45965G>T
(TTN)
|
XP_011510031.1:p.Arg15322Ile
|
|
XM_011511730.1:c.19859G>T
(TTN)
|
XP_011510032.1:p.Arg6620Ile
|
|
XM_011511731.1:c.19718G>T
(TTN)
|
XP_011510033.1:p.Arg6573Ile
|
|
XM_017004819.1:c.45761G>T
(TTN)
|
XP_016860308.1:p.Arg15254Ile
|
|
XM_017004820.1:c.41159G>T
(TTN)
|
XP_016860309.1:p.Arg13720Ile
|
|
XM_017004821.1:c.41156G>T
(TTN)
|
XP_016860310.1:p.Arg13719Ile
|
|
XM_017004822.1:c.38198G>T
(TTN)
|
XP_016860311.1:p.Arg12733Ile
|
|
XM_017004823.1:c.19814G>T
(TTN)
|
XP_016860312.1:p.Arg6605Ile
|
|
XM_024453094.1:c.41309G>T
(TTN)
|
XP_024308862.1:p.Arg13770Ile
|
|
XM_024453095.1:c.41306G>T
(TTN)
|
XP_024308863.1:p.Arg13769Ile
|
|
XM_024453096.1:c.40739G>T
(TTN)
|
XP_024308864.1:p.Arg13580Ile
|
|
XM_024453097.1:c.38081G>T
(TTN)
|
XP_024308865.1:p.Arg12694Ile
|
|
XM_024453098.1:c.38000G>T
(TTN)
|
XP_024308866.1:p.Arg12667Ile
|
|
XM_024453099.1:c.19763G>T
(TTN)
|
XP_024308867.1:p.Arg6588Ile
|
|
XM_024453100.1:c.9617G>T
(TTN)
|
XP_024308868.1:p.Arg3206Ile
|
|