ENST00000342992.11:c.69432A>C
(TTN)
|
ENSP00000343764.6:p.Arg23144Ser
|
|
ENST00000342175.11:c.50517A>C
(TTN)
|
ENSP00000340554.6:p.Arg16839Ser
|
|
ENST00000359218.10:c.50316A>C
(TTN)
|
ENSP00000352154.5:p.Arg16772Ser
|
|
ENST00000342175.10:c.50517A>C
(TTN)
|
ENSP00000340554.6:p.Arg16839Ser
|
|
ENST00000342992.10:c.69432A>C
(TTN)
|
ENSP00000343764.6:p.Arg23144Ser
|
|
ENST00000359218.9:c.50316A>C
(TTN)
|
ENSP00000352154.5:p.Arg16772Ser
|
|
ENST00000460472.6:c.49941A>C
(TTN)
|
ENSP00000434586.1:p.Arg16647Ser
|
|
ENST00000589042.5:c.77136A>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Arg25712Ser
|
|
ENST00000591111.5:c.72213A>C
(TTN)
|
ENSP00000465570.1:p.Arg24071Ser
|
|
ENST00000615779.4:c.72213A>C
(TTN)
|
ENSP00000483597.1:p.Arg24071Ser
|
|
NM_001256850.1:c.72213A>C
(TTN)
|
NP_001243779.1:p.Arg24071Ser
|
|
NM_001267550.2:c.77136A>C
(TTN)
MANE Select
|
NP_001254479.2:p.Arg25712Ser
|
|
NM_003319.4:c.49941A>C
(TTN)
|
NP_003310.4:p.Arg16647Ser
|
|
NM_133378.4:c.69432A>C
(TTN)
|
NP_596869.4:p.Arg23144Ser
|
|
NM_133432.3:c.50316A>C
(TTN)
|
NP_597676.3:p.Arg16772Ser
|
|
NM_133437.4:c.50517A>C
(TTN)
|
NP_597681.4:p.Arg16839Ser
|
|
NR_038271.1:n.447-2304T>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-13576T>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.76233A>C
(TTN)
|
XP_011510031.1:p.Arg25411Ser
|
|
XM_011511730.1:c.50127A>C
(TTN)
|
XP_011510032.1:p.Arg16709Ser
|
|
XM_011511731.1:c.49986A>C
(TTN)
|
XP_011510033.1:p.Arg16662Ser
|
|
XM_017004819.1:c.76029A>C
(TTN)
|
XP_016860308.1:p.Arg25343Ser
|
|
XM_017004820.1:c.71427A>C
(TTN)
|
XP_016860309.1:p.Arg23809Ser
|
|
XM_017004821.1:c.71424A>C
(TTN)
|
XP_016860310.1:p.Arg23808Ser
|
|
XM_017004822.1:c.68466A>C
(TTN)
|
XP_016860311.1:p.Arg22822Ser
|
|
XM_017004823.1:c.50082A>C
(TTN)
|
XP_016860312.1:p.Arg16694Ser
|
|
XM_024453094.1:c.71577A>C
(TTN)
|
XP_024308862.1:p.Arg23859Ser
|
|
XM_024453095.1:c.71574A>C
(TTN)
|
XP_024308863.1:p.Arg23858Ser
|
|
XM_024453096.1:c.71007A>C
(TTN)
|
XP_024308864.1:p.Arg23669Ser
|
|
XM_024453097.1:c.68349A>C
(TTN)
|
XP_024308865.1:p.Arg22783Ser
|
|
XM_024453098.1:c.68268A>C
(TTN)
|
XP_024308866.1:p.Arg22756Ser
|
|
XM_024453099.1:c.50031A>C
(TTN)
|
XP_024308867.1:p.Arg16677Ser
|
|
XM_024453100.1:c.39885A>C
(TTN)
|
XP_024308868.1:p.Arg13295Ser
|
|