ENST00000290866.10:c.3892G>C
MANE Select
|
ENSP00000290866.4:p.Gly1298Arg
|
|
ENST00000290863.10:c.2170G>C
|
ENSP00000290863.6:p.Gly724Arg
|
|
ENST00000290866.9:c.3892G>C
|
ENSP00000290866.4:p.Gly1298Arg
|
|
ENST00000413513.7:c.2047G>C
|
ENSP00000392247.3:p.Gly683Arg
|
|
ENST00000428043.5:c.*314G>C
|
ENSP00000397593.2:n.*314G>C
|
|
ENST00000577647.2:c.1969+352G>C
|
ENSP00000464149.1:n.1969+352G>C
|
|
ENST00000578839.5:c.*1647G>C
|
ENSP00000462110.2:n.*1647G>C
|
|
ENST00000579314.5:c.*1621G>C
|
ENSP00000462599.1:n.*1621G>C
|
|
NM_000789.3:c.3892G>C
|
NP_000780.1:p.Gly1298Arg
|
|
NM_001178057.1:c.2047G>C
|
NP_001171528.1:p.Gly683Arg
|
|
NM_152830.2:c.2170G>C
|
NP_690043.1:p.Gly724Arg
|
|
XM_005257110.1:c.3343G>C
|
XP_005257167.1:p.Gly1115Arg
|
|
XM_006721737.2:c.2230G>C
|
XP_006721800.2:p.Gly744Arg
|
|
XM_006721737.3:c.2230G>C
|
XP_006721800.2:p.Gly744Arg
|
|
NM_000789.4:c.3892G>C
MANE Select
|
NP_000780.1:p.Gly1298Arg
|
|
NM_001178057.2:c.2047G>C
|
NP_001171528.1:p.Gly683Arg
|
|
NM_152830.3:c.2170G>C
|
NP_690043.1:p.Gly724Arg
|
|
NM_001382700.1:c.3325G>C
|
NP_001369629.1:p.Gly1109Arg
|
|
NM_001382701.1:c.3040G>C
|
NP_001369630.1:p.Gly1014Arg
|
|
NM_001382702.1:c.1507G>C
|
NP_001369631.1:p.Gly503Arg
|
|
NR_168483.1:n.2270G>C
|
|
|