ENST00000342992.11:c.83354G>C
(TTN)
|
ENSP00000343764.6:p.Gly27785Ala
|
|
ENST00000342175.11:c.64439G>C
(TTN)
|
ENSP00000340554.6:p.Gly21480Ala
|
|
ENST00000359218.10:c.64238G>C
(TTN)
|
ENSP00000352154.5:p.Gly21413Ala
|
|
ENST00000342175.10:c.64439G>C
(TTN)
|
ENSP00000340554.6:p.Gly21480Ala
|
|
ENST00000342992.10:c.83354G>C
(TTN)
|
ENSP00000343764.6:p.Gly27785Ala
|
|
ENST00000359218.9:c.64238G>C
(TTN)
|
ENSP00000352154.5:p.Gly21413Ala
|
|
ENST00000460472.6:c.63863G>C
(TTN)
|
ENSP00000434586.1:p.Gly21288Ala
|
|
ENST00000589042.5:c.91058G>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gly30353Ala
|
|
ENST00000591111.5:c.86135G>C
(TTN)
|
ENSP00000465570.1:p.Gly28712Ala
|
|
ENST00000615779.4:c.86135G>C
(TTN)
|
ENSP00000483597.1:p.Gly28712Ala
|
|
NM_001256850.1:c.86135G>C
(TTN)
|
NP_001243779.1:p.Gly28712Ala
|
|
NM_001267550.2:c.91058G>C
(TTN)
MANE Select
|
NP_001254479.2:p.Gly30353Ala
|
|
NM_003319.4:c.63863G>C
(TTN)
|
NP_003310.4:p.Gly21288Ala
|
|
NM_133378.4:c.83354G>C
(TTN)
|
NP_596869.4:p.Gly27785Ala
|
|
NM_133432.3:c.64238G>C
(TTN)
|
NP_597676.3:p.Gly21413Ala
|
|
NM_133437.4:c.64439G>C
(TTN)
|
NP_597681.4:p.Gly21480Ala
|
|
NR_038271.1:n.447-19458C>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+9481C>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.90155G>C
(TTN)
|
XP_011510031.1:p.Gly30052Ala
|
|
XM_011511730.1:c.64049G>C
(TTN)
|
XP_011510032.1:p.Gly21350Ala
|
|
XM_011511731.1:c.63908G>C
(TTN)
|
XP_011510033.1:p.Gly21303Ala
|
|
XM_017004819.1:c.89951G>C
(TTN)
|
XP_016860308.1:p.Gly29984Ala
|
|
XM_017004820.1:c.85349G>C
(TTN)
|
XP_016860309.1:p.Gly28450Ala
|
|
XM_017004821.1:c.85346G>C
(TTN)
|
XP_016860310.1:p.Gly28449Ala
|
|
XM_017004822.1:c.82388G>C
(TTN)
|
XP_016860311.1:p.Gly27463Ala
|
|
XM_017004823.1:c.64004G>C
(TTN)
|
XP_016860312.1:p.Gly21335Ala
|
|
XM_024453094.1:c.85499G>C
(TTN)
|
XP_024308862.1:p.Gly28500Ala
|
|
XM_024453095.1:c.85496G>C
(TTN)
|
XP_024308863.1:p.Gly28499Ala
|
|
XM_024453096.1:c.84929G>C
(TTN)
|
XP_024308864.1:p.Gly28310Ala
|
|
XM_024453097.1:c.82271G>C
(TTN)
|
XP_024308865.1:p.Gly27424Ala
|
|
XM_024453098.1:c.82190G>C
(TTN)
|
XP_024308866.1:p.Gly27397Ala
|
|
XM_024453099.1:c.63953G>C
(TTN)
|
XP_024308867.1:p.Gly21318Ala
|
|
XM_024453100.1:c.53807G>C
(TTN)
|
XP_024308868.1:p.Gly17936Ala
|
|