ENST00000476274.7:n.953G>T
|
|
|
ENST00000643029.1:c.*2128G>T
|
ENSP00000496586.1:n.*2128G>T
|
|
ENST00000643338.1:c.*2017G>T
|
ENSP00000495890.1:n.*2017G>T
|
|
ENST00000644144.2:c.453G>T
MANE Select
|
ENSP00000494600.1:p.Glu151Asp
|
|
ENST00000645007.1:c.*2377G>T
|
ENSP00000494773.1:n.*2377G>T
|
|
ENST00000646171.1:c.*486G>T
|
ENSP00000495484.1:n.*486G>T
|
|
ENST00000223836.10:c.501G>T
|
ENSP00000223836.10:p.Glu167Asp
|
|
ENST00000373156.5:c.453G>T
|
ENSP00000362249.1:p.Glu151Asp
|
|
ENST00000373176.5:c.453G>T
|
ENSP00000362271.1:p.Glu151Asp
|
|
ENST00000413016.5:c.275G>T
|
|
|
ENST00000550143.5:c.233G>T
|
ENSP00000449130.1:n.233G>T
|
|
NM_000476.2:c.453G>T
|
NP_000467.1:p.Glu151Asp
|
|
XM_005251786.2:c.501G>T
|
XP_005251843.1:p.Glu167Asp
|
|
XM_011518348.1:c.453G>T
|
XP_011516650.1:p.Glu151Asp
|
|
XM_011518349.1:c.273G>T
|
XP_011516651.1:p.Glu91Asp
|
|
NM_001318121.1:c.453G>T
|
NP_001305050.1:p.Glu151Asp
|
|
NM_001318122.1:c.501G>T
|
NP_001305051.1:p.Glu167Asp
|
|
XM_017014428.1:c.453G>T
|
XP_016869917.1:p.Glu151Asp
|
|
XM_024447439.1:c.432G>T
|
XP_024303207.1:p.Glu144Asp
|
|
XM_024447440.1:c.273G>T
|
XP_024303208.1:p.Glu91Asp
|
|
NM_001318122.2:c.501G>T
|
NP_001305051.1:p.Glu167Asp
|
|
NM_000476.3:c.453G>T
MANE Select
|
NP_000467.1:p.Glu151Asp
|
|
NR_174625.1:n.3772G>T
|
|
|
NR_174626.1:n.3615G>T
|
|
|
NR_174627.1:n.3652G>T
|
|
|
NR_174628.1:n.3030G>T
|
|
|
NR_174629.1:n.2975G>T
|
|
|
NR_174630.1:n.3011G>T
|
|
|
NR_174631.1:n.2956G>T
|
|
|
NR_174632.1:n.3045G>T
|
|
|