ENST00000297598.5:c.842G>A
MANE Select
|
ENSP00000297598.4:p.Gly281Asp
|
|
ENST00000297598.4:c.842G>A
|
ENSP00000297598.4:p.Gly281Asp
|
|
ENST00000396200.3:c.917G>A
|
ENSP00000379503.3:p.Gly306Asp
|
|
ENST00000517764.1:c.842G>A
|
ENSP00000430380.1:p.Gly281Asp
|
|
ENST00000520728.5:c.842G>A
|
ENSP00000428317.1:p.Gly281Asp
|
|
NM_001161779.1:c.917G>A
|
NP_001155251.1:p.Gly306Asp
|
|
NM_001161780.1:c.917G>A
|
NP_001155252.1:p.Gly306Asp
|
|
NM_001161781.1:c.842G>A
|
NP_001155253.1:p.Gly281Asp
|
|
NM_018444.3:c.842G>A
|
NP_060914.2:p.Gly281Asp
|
|
XM_011517135.1:c.896G>A
|
XP_011515437.1:p.Gly299Asp
|
|
XM_011517136.1:c.842G>A
|
XP_011515438.1:p.Gly281Asp
|
|
XM_011517137.1:c.842G>A
|
XP_011515439.1:p.Gly281Asp
|
|
XM_011517135.2:c.896G>A
|
XP_011515437.1:p.Gly299Asp
|
|
XM_011517136.2:c.842G>A
|
XP_011515438.1:p.Gly281Asp
|
|
XM_017013588.1:c.1004G>A
|
XP_016869077.1:p.Gly335Asp
|
|
NM_018444.4:c.842G>A
MANE Select
|
NP_060914.2:p.Gly281Asp
|
|
NM_001161780.2:c.917G>A
|
NP_001155252.1:p.Gly306Asp
|
|
NM_001161781.2:c.842G>A
|
NP_001155253.1:p.Gly281Asp
|
|
NM_001161779.2:c.917G>A
|
NP_001155251.1:p.Gly306Asp
|
|