ENST00000342992.11:c.63627A>C
(TTN)
|
ENSP00000343764.6:p.Leu21209Phe
|
|
ENST00000342175.11:c.44712A>C
(TTN)
|
ENSP00000340554.6:p.Leu14904Phe
|
|
ENST00000359218.10:c.44511A>C
(TTN)
|
ENSP00000352154.5:p.Leu14837Phe
|
|
ENST00000342175.10:c.44712A>C
(TTN)
|
ENSP00000340554.6:p.Leu14904Phe
|
|
ENST00000342992.10:c.63627A>C
(TTN)
|
ENSP00000343764.6:p.Leu21209Phe
|
|
ENST00000359218.9:c.44511A>C
(TTN)
|
ENSP00000352154.5:p.Leu14837Phe
|
|
ENST00000460472.6:c.44136A>C
(TTN)
|
ENSP00000434586.1:p.Leu14712Phe
|
|
ENST00000589042.5:c.71331A>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu23777Phe
|
|
ENST00000591111.5:c.66408A>C
(TTN)
|
ENSP00000465570.1:p.Leu22136Phe
|
|
ENST00000615779.4:c.66408A>C
(TTN)
|
ENSP00000483597.1:p.Leu22136Phe
|
|
NM_001256850.1:c.66408A>C
(TTN)
|
NP_001243779.1:p.Leu22136Phe
|
|
NM_001267550.2:c.71331A>C
(TTN)
MANE Select
|
NP_001254479.2:p.Leu23777Phe
|
|
NM_003319.4:c.44136A>C
(TTN)
|
NP_003310.4:p.Leu14712Phe
|
|
NM_133378.4:c.63627A>C
(TTN)
|
NP_596869.4:p.Leu21209Phe
|
|
NM_133432.3:c.44511A>C
(TTN)
|
NP_597676.3:p.Leu14837Phe
|
|
NM_133437.4:c.44712A>C
(TTN)
|
NP_597681.4:p.Leu14904Phe
|
|
NR_038271.1:n.596+3352T>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-7771T>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.70428A>C
(TTN)
|
XP_011510031.1:p.Leu23476Phe
|
|
XM_011511730.1:c.44322A>C
(TTN)
|
XP_011510032.1:p.Leu14774Phe
|
|
XM_011511731.1:c.44181A>C
(TTN)
|
XP_011510033.1:p.Leu14727Phe
|
|
XM_017004819.1:c.70224A>C
(TTN)
|
XP_016860308.1:p.Leu23408Phe
|
|
XM_017004820.1:c.65622A>C
(TTN)
|
XP_016860309.1:p.Leu21874Phe
|
|
XM_017004821.1:c.65619A>C
(TTN)
|
XP_016860310.1:p.Leu21873Phe
|
|
XM_017004822.1:c.62661A>C
(TTN)
|
XP_016860311.1:p.Leu20887Phe
|
|
XM_017004823.1:c.44277A>C
(TTN)
|
XP_016860312.1:p.Leu14759Phe
|
|
XM_024453094.1:c.65772A>C
(TTN)
|
XP_024308862.1:p.Leu21924Phe
|
|
XM_024453095.1:c.65769A>C
(TTN)
|
XP_024308863.1:p.Leu21923Phe
|
|
XM_024453096.1:c.65202A>C
(TTN)
|
XP_024308864.1:p.Leu21734Phe
|
|
XM_024453097.1:c.62544A>C
(TTN)
|
XP_024308865.1:p.Leu20848Phe
|
|
XM_024453098.1:c.62463A>C
(TTN)
|
XP_024308866.1:p.Leu20821Phe
|
|
XM_024453099.1:c.44226A>C
(TTN)
|
XP_024308867.1:p.Leu14742Phe
|
|
XM_024453100.1:c.34080A>C
(TTN)
|
XP_024308868.1:p.Leu11360Phe
|
|