ENST00000342992.11:c.44035G>C
(TTN)
|
ENSP00000343764.6:p.Asp14679His
|
|
ENST00000342175.11:c.25120G>C
(TTN)
|
ENSP00000340554.6:p.Asp8374His
|
|
ENST00000359218.10:c.24919G>C
(TTN)
|
ENSP00000352154.5:p.Asp8307His
|
|
ENST00000342175.10:c.25120G>C
(TTN)
|
ENSP00000340554.6:p.Asp8374His
|
|
ENST00000342992.10:c.44035G>C
(TTN)
|
ENSP00000343764.6:p.Asp14679His
|
|
ENST00000359218.9:c.24919G>C
(TTN)
|
ENSP00000352154.5:p.Asp8307His
|
|
ENST00000460472.6:c.24544G>C
(TTN)
|
ENSP00000434586.1:p.Asp8182His
|
|
ENST00000589042.5:c.51739G>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp17247His
|
|
ENST00000591111.5:c.46816G>C
(TTN)
|
ENSP00000465570.1:p.Asp15606His
|
|
ENST00000615779.4:c.46816G>C
(TTN)
|
ENSP00000483597.1:p.Asp15606His
|
|
NM_001256850.1:c.46816G>C
(TTN)
|
NP_001243779.1:p.Asp15606His
|
|
NM_001267550.2:c.51739G>C
(TTN)
MANE Select
|
NP_001254479.2:p.Asp17247His
|
|
NM_003319.4:c.24544G>C
(TTN)
|
NP_003310.4:p.Asp8182His
|
|
NM_133378.4:c.44035G>C
(TTN)
|
NP_596869.4:p.Asp14679His
|
|
NM_133432.3:c.24919G>C
(TTN)
|
NP_597676.3:p.Asp8307His
|
|
NM_133437.4:c.25120G>C
(TTN)
|
NP_597681.4:p.Asp8374His
|
|
NR_038271.1:n.782+1418C>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.50836G>C
(TTN)
|
XP_011510031.1:p.Asp16946His
|
|
XM_011511730.1:c.24730G>C
(TTN)
|
XP_011510032.1:p.Asp8244His
|
|
XM_011511731.1:c.24589G>C
(TTN)
|
XP_011510033.1:p.Asp8197His
|
|
XM_017004819.1:c.50632G>C
(TTN)
|
XP_016860308.1:p.Asp16878His
|
|
XM_017004820.1:c.46030G>C
(TTN)
|
XP_016860309.1:p.Asp15344His
|
|
XM_017004821.1:c.46027G>C
(TTN)
|
XP_016860310.1:p.Asp15343His
|
|
XM_017004822.1:c.43069G>C
(TTN)
|
XP_016860311.1:p.Asp14357His
|
|
XM_017004823.1:c.24685G>C
(TTN)
|
XP_016860312.1:p.Asp8229His
|
|
XM_024453094.1:c.46180G>C
(TTN)
|
XP_024308862.1:p.Asp15394His
|
|
XM_024453095.1:c.46177G>C
(TTN)
|
XP_024308863.1:p.Asp15393His
|
|
XM_024453096.1:c.45610G>C
(TTN)
|
XP_024308864.1:p.Asp15204His
|
|
XM_024453097.1:c.42952G>C
(TTN)
|
XP_024308865.1:p.Asp14318His
|
|
XM_024453098.1:c.42871G>C
(TTN)
|
XP_024308866.1:p.Asp14291His
|
|
XM_024453099.1:c.24634G>C
(TTN)
|
XP_024308867.1:p.Asp8212His
|
|
XM_024453100.1:c.14488G>C
(TTN)
|
XP_024308868.1:p.Asp4830His
|
|