ENST00000397801.6:c.4010G>A
MANE Select
|
ENSP00000380903.1:p.Gly1337Asp
|
|
ENST00000397801.5:c.4010G>A
|
ENSP00000380903.1:p.Gly1337Asp
|
|
ENST00000524971.1:n.909G>A
|
|
|
ENST00000525304.5:n.830G>A
|
|
|
ENST00000525448.5:n.1772G>A
|
|
|
ENST00000525482.5:n.1279G>A
|
|
|
ENST00000527196.5:n.1571G>A
|
|
|
ENST00000527245.5:n.2888G>A
|
|
|
ENST00000529658.5:n.1905G>A
|
|
|
ENST00000538940.5:c.3944G>A
|
ENSP00000441797.1:p.Gly1315Asp
|
|
ENST00000543966.5:c.299G>A
|
ENSP00000438799.1:p.Gly100Asp
|
|
NM_022370.3:c.4010G>A
|
NP_071765.2:p.Gly1337Asp
|
|
XM_011542953.1:c.4982G>A
|
XP_011541255.1:p.Gly1661Asp
|
|
XM_017018122.1:c.3944G>A
|
XP_016873611.1:p.Gly1315Asp
|
|
NM_022370.4:c.4010G>A
MANE Select
|
NP_071765.2:p.Gly1337Asp
|
|
NM_001370356.1:c.1157G>A
|
NP_001357285.1:p.Gly386Asp
|
|
NM_001370357.1:c.1157G>A
|
NP_001357286.1:p.Gly386Asp
|
|
NM_001370358.1:c.1157G>A
|
NP_001357287.1:p.Gly386Asp
|
|
NM_001370359.1:c.1157G>A
|
NP_001357288.1:p.Gly386Asp
|
|
NM_001370361.1:c.1157G>A
|
NP_001357290.1:p.Gly386Asp
|
|
NM_001370364.1:c.962G>A
|
NP_001357293.1:p.Gly321Asp
|
|
NM_001370366.1:c.962G>A
|
NP_001357295.1:p.Gly321Asp
|
|
NR_163409.1:n.1158G>A
|
|
|
NR_163410.1:n.1249G>A
|
|
|
NR_163411.1:n.1401G>A
|
|
|
NR_163412.1:n.1444G>A
|
|
|
NR_163413.1:n.974G>A
|
|
|
NR_163414.1:n.1225G>A
|
|
|
NR_163415.1:n.779G>A
|
|
|