ENST00000290866.10:c.2157G>A
MANE Select
|
ENSP00000290866.4:p.Arg719=
|
|
ENST00000290863.10:c.435G>A
|
ENSP00000290863.6:p.Arg145=
|
|
ENST00000290866.9:c.2157G>A
|
ENSP00000290866.4:p.Arg719=
|
|
ENST00000413513.7:c.435G>A
|
ENSP00000392247.3:p.Arg145=
|
|
ENST00000428043.5:c.2157G>A
|
ENSP00000397593.2:p.Arg719=
|
|
ENST00000577647.2:c.435G>A
|
ENSP00000464149.1:p.Arg145=
|
|
ENST00000578839.5:c.*227G>A
|
ENSP00000462110.2:n.*227G>A
|
|
ENST00000579204.1:c.338G>A
|
ENSP00000464629.1:n.338G>A
|
|
ENST00000579314.5:c.435G>A
|
ENSP00000462599.1:p.Arg145=
|
|
ENST00000579726.5:c.719G>A
|
|
|
ENST00000582005.5:c.*77G>A
|
ENSP00000462002.1:n.*77G>A
|
|
NM_000789.3:c.2157G>A
|
NP_000780.1:p.Arg719=
|
|
NM_001178057.1:c.435G>A
|
NP_001171528.1:p.Arg145=
|
|
NM_152830.2:c.435G>A
|
NP_690043.1:p.Arg145=
|
|
XM_005257110.1:c.1608G>A
|
XP_005257167.1:p.Arg536=
|
|
XM_006721737.2:c.495G>A
|
XP_006721800.2:p.Arg165=
|
|
XM_006721737.3:c.495G>A
|
XP_006721800.2:p.Arg165=
|
|
NM_000789.4:c.2157G>A
MANE Select
|
NP_000780.1:p.Arg719=
|
|
NM_001178057.2:c.435G>A
|
NP_001171528.1:p.Arg145=
|
|
NM_152830.3:c.435G>A
|
NP_690043.1:p.Arg145=
|
|
NM_001382700.1:c.1590G>A
|
NP_001369629.1:p.Arg530=
|
|
NM_001382701.1:c.1305G>A
|
NP_001369630.1:p.Arg435=
|
|
NM_001382702.1:c.87G>A
|
NP_001369631.1:p.Arg29=
|
|
NR_168483.1:n.457G>A
|
|
|