ENST00000342992.11:c.39547G>A
(TTN)
|
ENSP00000343764.6:p.Glu13183Lys
|
|
ENST00000342175.11:c.20632G>A
(TTN)
|
ENSP00000340554.6:p.Glu6878Lys
|
|
ENST00000359218.10:c.20431G>A
(TTN)
|
ENSP00000352154.5:p.Glu6811Lys
|
|
ENST00000342175.10:c.20632G>A
(TTN)
|
ENSP00000340554.6:p.Glu6878Lys
|
|
ENST00000342992.10:c.39547G>A
(TTN)
|
ENSP00000343764.6:p.Glu13183Lys
|
|
ENST00000359218.9:c.20431G>A
(TTN)
|
ENSP00000352154.5:p.Glu6811Lys
|
|
ENST00000460472.6:c.20056G>A
(TTN)
|
ENSP00000434586.1:p.Glu6686Lys
|
|
ENST00000589042.5:c.47251G>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu15751Lys
|
|
ENST00000591111.5:c.42328G>A
(TTN)
|
ENSP00000465570.1:p.Glu14110Lys
|
|
ENST00000615779.4:c.42328G>A
(TTN)
|
ENSP00000483597.1:p.Glu14110Lys
|
|
NM_001256850.1:c.42328G>A
(TTN)
|
NP_001243779.1:p.Glu14110Lys
|
|
NM_001267550.2:c.47251G>A
(TTN)
MANE Select
|
NP_001254479.2:p.Glu15751Lys
|
|
NM_003319.4:c.20056G>A
(TTN)
|
NP_003310.4:p.Glu6686Lys
|
|
NM_133378.4:c.39547G>A
(TTN)
|
NP_596869.4:p.Glu13183Lys
|
|
NM_133432.3:c.20431G>A
(TTN)
|
NP_597676.3:p.Glu6811Lys
|
|
NM_133437.4:c.20632G>A
(TTN)
|
NP_597681.4:p.Glu6878Lys
|
|
NR_038271.1:n.1605-1546C>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.46348G>A
(TTN)
|
XP_011510031.1:p.Glu15450Lys
|
|
XM_011511730.1:c.20242G>A
(TTN)
|
XP_011510032.1:p.Glu6748Lys
|
|
XM_011511731.1:c.20101G>A
(TTN)
|
XP_011510033.1:p.Glu6701Lys
|
|
XM_017004819.1:c.46144G>A
(TTN)
|
XP_016860308.1:p.Glu15382Lys
|
|
XM_017004820.1:c.41542G>A
(TTN)
|
XP_016860309.1:p.Glu13848Lys
|
|
XM_017004821.1:c.41539G>A
(TTN)
|
XP_016860310.1:p.Glu13847Lys
|
|
XM_017004822.1:c.38581G>A
(TTN)
|
XP_016860311.1:p.Glu12861Lys
|
|
XM_017004823.1:c.20197G>A
(TTN)
|
XP_016860312.1:p.Glu6733Lys
|
|
XM_024453094.1:c.41692G>A
(TTN)
|
XP_024308862.1:p.Glu13898Lys
|
|
XM_024453095.1:c.41689G>A
(TTN)
|
XP_024308863.1:p.Glu13897Lys
|
|
XM_024453096.1:c.41122G>A
(TTN)
|
XP_024308864.1:p.Glu13708Lys
|
|
XM_024453097.1:c.38464G>A
(TTN)
|
XP_024308865.1:p.Glu12822Lys
|
|
XM_024453098.1:c.38383G>A
(TTN)
|
XP_024308866.1:p.Glu12795Lys
|
|
XM_024453099.1:c.20146G>A
(TTN)
|
XP_024308867.1:p.Glu6716Lys
|
|
XM_024453100.1:c.10000G>A
(TTN)
|
XP_024308868.1:p.Glu3334Lys
|
|