ENST00000342992.11:c.53004G>C
(TTN)
|
ENSP00000343764.6:p.Leu17668=
|
|
ENST00000342175.11:c.34089G>C
(TTN)
|
ENSP00000340554.6:p.Leu11363=
|
|
ENST00000359218.10:c.33888G>C
(TTN)
|
ENSP00000352154.5:p.Leu11296=
|
|
ENST00000342175.10:c.34089G>C
(TTN)
|
ENSP00000340554.6:p.Leu11363=
|
|
ENST00000342992.10:c.53004G>C
(TTN)
|
ENSP00000343764.6:p.Leu17668=
|
|
ENST00000359218.9:c.33888G>C
(TTN)
|
ENSP00000352154.5:p.Leu11296=
|
|
ENST00000460472.6:c.33513G>C
(TTN)
|
ENSP00000434586.1:p.Leu11171=
|
|
ENST00000589042.5:c.60708G>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu20236=
|
|
ENST00000591111.5:c.55785G>C
(TTN)
|
ENSP00000465570.1:p.Leu18595=
|
|
ENST00000615779.4:c.55785G>C
(TTN)
|
ENSP00000483597.1:p.Leu18595=
|
|
NM_001256850.1:c.55785G>C
(TTN)
|
NP_001243779.1:p.Leu18595=
|
|
NM_001267550.2:c.60708G>C
(TTN)
MANE Select
|
NP_001254479.2:p.Leu20236=
|
|
NM_003319.4:c.33513G>C
(TTN)
|
NP_003310.4:p.Leu11171=
|
|
NM_133378.4:c.53004G>C
(TTN)
|
NP_596869.4:p.Leu17668=
|
|
NM_133432.3:c.33888G>C
(TTN)
|
NP_597676.3:p.Leu11296=
|
|
NM_133437.4:c.34089G>C
(TTN)
|
NP_597681.4:p.Leu11363=
|
|
NR_038271.1:n.597-6579C>G
(TTN-AS1)
|
|
|
NR_038272.1:n.3189-122C>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.59805G>C
(TTN)
|
XP_011510031.1:p.Leu19935=
|
|
XM_011511730.1:c.33699G>C
(TTN)
|
XP_011510032.1:p.Leu11233=
|
|
XM_011511731.1:c.33558G>C
(TTN)
|
XP_011510033.1:p.Leu11186=
|
|
XM_017004819.1:c.59601G>C
(TTN)
|
XP_016860308.1:p.Leu19867=
|
|
XM_017004820.1:c.54999G>C
(TTN)
|
XP_016860309.1:p.Leu18333=
|
|
XM_017004821.1:c.54996G>C
(TTN)
|
XP_016860310.1:p.Leu18332=
|
|
XM_017004822.1:c.52038G>C
(TTN)
|
XP_016860311.1:p.Leu17346=
|
|
XM_017004823.1:c.33654G>C
(TTN)
|
XP_016860312.1:p.Leu11218=
|
|
XM_024453094.1:c.55149G>C
(TTN)
|
XP_024308862.1:p.Leu18383=
|
|
XM_024453095.1:c.55146G>C
(TTN)
|
XP_024308863.1:p.Leu18382=
|
|
XM_024453096.1:c.54579G>C
(TTN)
|
XP_024308864.1:p.Leu18193=
|
|
XM_024453097.1:c.51921G>C
(TTN)
|
XP_024308865.1:p.Leu17307=
|
|
XM_024453098.1:c.51840G>C
(TTN)
|
XP_024308866.1:p.Leu17280=
|
|
XM_024453099.1:c.33603G>C
(TTN)
|
XP_024308867.1:p.Leu11201=
|
|
XM_024453100.1:c.23457G>C
(TTN)
|
XP_024308868.1:p.Leu7819=
|
|