ENST00000342992.11:c.60026A>C
(TTN)
|
ENSP00000343764.6:p.Lys20009Thr
|
|
ENST00000342175.11:c.41111A>C
(TTN)
|
ENSP00000340554.6:p.Lys13704Thr
|
|
ENST00000359218.10:c.40910A>C
(TTN)
|
ENSP00000352154.5:p.Lys13637Thr
|
|
ENST00000342175.10:c.41111A>C
(TTN)
|
ENSP00000340554.6:p.Lys13704Thr
|
|
ENST00000342992.10:c.60026A>C
(TTN)
|
ENSP00000343764.6:p.Lys20009Thr
|
|
ENST00000359218.9:c.40910A>C
(TTN)
|
ENSP00000352154.5:p.Lys13637Thr
|
|
ENST00000460472.6:c.40535A>C
(TTN)
|
ENSP00000434586.1:p.Lys13512Thr
|
|
ENST00000589042.5:c.67730A>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Lys22577Thr
|
|
ENST00000591111.5:c.62807A>C
(TTN)
|
ENSP00000465570.1:p.Lys20936Thr
|
|
ENST00000615779.4:c.62807A>C
(TTN)
|
ENSP00000483597.1:p.Lys20936Thr
|
|
NM_001256850.1:c.62807A>C
(TTN)
|
NP_001243779.1:p.Lys20936Thr
|
|
NM_001267550.2:c.67730A>C
(TTN)
MANE Select
|
NP_001254479.2:p.Lys22577Thr
|
|
NM_003319.4:c.40535A>C
(TTN)
|
NP_003310.4:p.Lys13512Thr
|
|
NM_133378.4:c.60026A>C
(TTN)
|
NP_596869.4:p.Lys20009Thr
|
|
NM_133432.3:c.40910A>C
(TTN)
|
NP_597676.3:p.Lys13637Thr
|
|
NM_133437.4:c.41111A>C
(TTN)
|
NP_597681.4:p.Lys13704Thr
|
|
NR_038271.1:n.596+7851T>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-3272T>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.66827A>C
(TTN)
|
XP_011510031.1:p.Lys22276Thr
|
|
XM_011511730.1:c.40721A>C
(TTN)
|
XP_011510032.1:p.Lys13574Thr
|
|
XM_011511731.1:c.40580A>C
(TTN)
|
XP_011510033.1:p.Lys13527Thr
|
|
XM_017004819.1:c.66623A>C
(TTN)
|
XP_016860308.1:p.Lys22208Thr
|
|
XM_017004820.1:c.62021A>C
(TTN)
|
XP_016860309.1:p.Lys20674Thr
|
|
XM_017004821.1:c.62018A>C
(TTN)
|
XP_016860310.1:p.Lys20673Thr
|
|
XM_017004822.1:c.59060A>C
(TTN)
|
XP_016860311.1:p.Lys19687Thr
|
|
XM_017004823.1:c.40676A>C
(TTN)
|
XP_016860312.1:p.Lys13559Thr
|
|
XM_024453094.1:c.62171A>C
(TTN)
|
XP_024308862.1:p.Lys20724Thr
|
|
XM_024453095.1:c.62168A>C
(TTN)
|
XP_024308863.1:p.Lys20723Thr
|
|
XM_024453096.1:c.61601A>C
(TTN)
|
XP_024308864.1:p.Lys20534Thr
|
|
XM_024453097.1:c.58943A>C
(TTN)
|
XP_024308865.1:p.Lys19648Thr
|
|
XM_024453098.1:c.58862A>C
(TTN)
|
XP_024308866.1:p.Lys19621Thr
|
|
XM_024453099.1:c.40625A>C
(TTN)
|
XP_024308867.1:p.Lys13542Thr
|
|
XM_024453100.1:c.30479A>C
(TTN)
|
XP_024308868.1:p.Lys10160Thr
|
|