ENST00000342992.11:c.39165A>T
(TTN)
|
ENSP00000343764.6:p.Arg13055Ser
|
|
ENST00000342175.11:c.20250A>T
(TTN)
|
ENSP00000340554.6:p.Arg6750Ser
|
|
ENST00000359218.10:c.20049A>T
(TTN)
|
ENSP00000352154.5:p.Arg6683Ser
|
|
ENST00000342175.10:c.20250A>T
(TTN)
|
ENSP00000340554.6:p.Arg6750Ser
|
|
ENST00000342992.10:c.39165A>T
(TTN)
|
ENSP00000343764.6:p.Arg13055Ser
|
|
ENST00000359218.9:c.20049A>T
(TTN)
|
ENSP00000352154.5:p.Arg6683Ser
|
|
ENST00000460472.6:c.19674A>T
(TTN)
|
ENSP00000434586.1:p.Arg6558Ser
|
|
ENST00000589042.5:c.46869A>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Arg15623Ser
|
|
ENST00000591111.5:c.41946A>T
(TTN)
|
ENSP00000465570.1:p.Arg13982Ser
|
|
ENST00000615779.4:c.41946A>T
(TTN)
|
ENSP00000483597.1:p.Arg13982Ser
|
|
NM_001256850.1:c.41946A>T
(TTN)
|
NP_001243779.1:p.Arg13982Ser
|
|
NM_001267550.2:c.46869A>T
(TTN)
MANE Select
|
NP_001254479.2:p.Arg15623Ser
|
|
NM_003319.4:c.19674A>T
(TTN)
|
NP_003310.4:p.Arg6558Ser
|
|
NM_133378.4:c.39165A>T
(TTN)
|
NP_596869.4:p.Arg13055Ser
|
|
NM_133432.3:c.20049A>T
(TTN)
|
NP_597676.3:p.Arg6683Ser
|
|
NM_133437.4:c.20250A>T
(TTN)
|
NP_597681.4:p.Arg6750Ser
|
|
NR_038271.1:n.1605-1072T>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.45966A>T
(TTN)
|
XP_011510031.1:p.Arg15322Ser
|
|
XM_011511730.1:c.19860A>T
(TTN)
|
XP_011510032.1:p.Arg6620Ser
|
|
XM_011511731.1:c.19719A>T
(TTN)
|
XP_011510033.1:p.Arg6573Ser
|
|
XM_017004819.1:c.45762A>T
(TTN)
|
XP_016860308.1:p.Arg15254Ser
|
|
XM_017004820.1:c.41160A>T
(TTN)
|
XP_016860309.1:p.Arg13720Ser
|
|
XM_017004821.1:c.41157A>T
(TTN)
|
XP_016860310.1:p.Arg13719Ser
|
|
XM_017004822.1:c.38199A>T
(TTN)
|
XP_016860311.1:p.Arg12733Ser
|
|
XM_017004823.1:c.19815A>T
(TTN)
|
XP_016860312.1:p.Arg6605Ser
|
|
XM_024453094.1:c.41310A>T
(TTN)
|
XP_024308862.1:p.Arg13770Ser
|
|
XM_024453095.1:c.41307A>T
(TTN)
|
XP_024308863.1:p.Arg13769Ser
|
|
XM_024453096.1:c.40740A>T
(TTN)
|
XP_024308864.1:p.Arg13580Ser
|
|
XM_024453097.1:c.38082A>T
(TTN)
|
XP_024308865.1:p.Arg12694Ser
|
|
XM_024453098.1:c.38001A>T
(TTN)
|
XP_024308866.1:p.Arg12667Ser
|
|
XM_024453099.1:c.19764A>T
(TTN)
|
XP_024308867.1:p.Arg6588Ser
|
|
XM_024453100.1:c.9618A>T
(TTN)
|
XP_024308868.1:p.Arg3206Ser
|
|