ENST00000342992.11:c.41271C>A
(TTN)
|
ENSP00000343764.6:p.Asp13757Glu
|
|
ENST00000342175.11:c.22356C>A
(TTN)
|
ENSP00000340554.6:p.Asp7452Glu
|
|
ENST00000359218.10:c.22155C>A
(TTN)
|
ENSP00000352154.5:p.Asp7385Glu
|
|
ENST00000342175.10:c.22356C>A
(TTN)
|
ENSP00000340554.6:p.Asp7452Glu
|
|
ENST00000342992.10:c.41271C>A
(TTN)
|
ENSP00000343764.6:p.Asp13757Glu
|
|
ENST00000359218.9:c.22155C>A
(TTN)
|
ENSP00000352154.5:p.Asp7385Glu
|
|
ENST00000460472.6:c.21780C>A
(TTN)
|
ENSP00000434586.1:p.Asp7260Glu
|
|
ENST00000589042.5:c.48975C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp16325Glu
|
|
ENST00000591111.5:c.44052C>A
(TTN)
|
ENSP00000465570.1:p.Asp14684Glu
|
|
ENST00000615779.4:c.44052C>A
(TTN)
|
ENSP00000483597.1:p.Asp14684Glu
|
|
NM_001256850.1:c.44052C>A
(TTN)
|
NP_001243779.1:p.Asp14684Glu
|
|
NM_001267550.2:c.48975C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Asp16325Glu
|
|
NM_003319.4:c.21780C>A
(TTN)
|
NP_003310.4:p.Asp7260Glu
|
|
NM_133378.4:c.41271C>A
(TTN)
|
NP_596869.4:p.Asp13757Glu
|
|
NM_133432.3:c.22155C>A
(TTN)
|
NP_597676.3:p.Asp7385Glu
|
|
NM_133437.4:c.22356C>A
(TTN)
|
NP_597681.4:p.Asp7452Glu
|
|
NR_038271.1:n.1287G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.48072C>A
(TTN)
|
XP_011510031.1:p.Asp16024Glu
|
|
XM_011511730.1:c.21966C>A
(TTN)
|
XP_011510032.1:p.Asp7322Glu
|
|
XM_011511731.1:c.21825C>A
(TTN)
|
XP_011510033.1:p.Asp7275Glu
|
|
XM_017004819.1:c.47868C>A
(TTN)
|
XP_016860308.1:p.Asp15956Glu
|
|
XM_017004820.1:c.43266C>A
(TTN)
|
XP_016860309.1:p.Asp14422Glu
|
|
XM_017004821.1:c.43263C>A
(TTN)
|
XP_016860310.1:p.Asp14421Glu
|
|
XM_017004822.1:c.40305C>A
(TTN)
|
XP_016860311.1:p.Asp13435Glu
|
|
XM_017004823.1:c.21921C>A
(TTN)
|
XP_016860312.1:p.Asp7307Glu
|
|
XM_024453094.1:c.43416C>A
(TTN)
|
XP_024308862.1:p.Asp14472Glu
|
|
XM_024453095.1:c.43413C>A
(TTN)
|
XP_024308863.1:p.Asp14471Glu
|
|
XM_024453096.1:c.42846C>A
(TTN)
|
XP_024308864.1:p.Asp14282Glu
|
|
XM_024453097.1:c.40188C>A
(TTN)
|
XP_024308865.1:p.Asp13396Glu
|
|
XM_024453098.1:c.40107C>A
(TTN)
|
XP_024308866.1:p.Asp13369Glu
|
|
XM_024453099.1:c.21870C>A
(TTN)
|
XP_024308867.1:p.Asp7290Glu
|
|
XM_024453100.1:c.11724C>A
(TTN)
|
XP_024308868.1:p.Asp3908Glu
|
|