ENST00000651671.1:c.6378A>G
MANE Select
|
ENSP00000498587.1:p.Gly2126=
|
|
ENST00000679595.1:c.*1418A>G
|
ENSP00000506241.1:n.*1418A>G
|
|
ENST00000679969.1:n.2974A>G
|
|
|
ENST00000680003.1:n.2710A>G
|
|
|
ENST00000680133.1:c.6264A>G
|
ENSP00000505319.1:p.Gly2088=
|
|
ENST00000680218.1:c.6258A>G
|
ENSP00000505339.1:p.Gly2086=
|
|
ENST00000680668.1:c.6264A>G
|
ENSP00000506336.1:p.Gly2088=
|
|
ENST00000680778.1:c.3975A>G
|
ENSP00000506033.1:p.Gly1325=
|
|
ENST00000680924.1:c.*3778A>G
|
ENSP00000506031.1:n.*3778A>G
|
|
ENST00000681135.1:c.*3987A>G
|
ENSP00000506636.1:n.*3987A>G
|
|
ENST00000681298.1:n.4483A>G
|
|
|
ENST00000681454.1:c.*5614A>G
|
ENSP00000505763.1:n.*5614A>G
|
|
ENST00000277541.6:c.6378A>G
|
ENSP00000277541.6:p.Gly2126=
|
|
NM_017617.3:c.6378A>G
|
NP_060087.3:p.Gly2126=
|
|
XM_011518717.1:c.5679A>G
|
XP_011517019.1:p.Gly1893=
|
|
NM_017617.5:c.6378A>G
MANE Select
|
NP_060087.3:p.Gly2126=
|
|
XM_011518717.2:c.5655A>G
|
XP_011517019.2:p.Gly1885=
|
|