ENST00000290866.10:c.2266G=
MANE Select
|
ENSP00000290866.4:p.Val756=
|
|
ENST00000290863.10:c.544G=
|
ENSP00000290863.6:p.Val182=
|
|
ENST00000290866.9:c.2266G=
|
ENSP00000290866.4:p.Val756=
|
|
ENST00000413513.7:c.544G=
|
ENSP00000392247.3:p.Val182=
|
|
ENST00000428043.5:c.2266G=
|
ENSP00000397593.2:p.Val756=
|
|
ENST00000577647.2:c.544G=
|
ENSP00000464149.1:p.Val182=
|
|
ENST00000578839.5:c.*336G=
|
ENSP00000462110.2:n.*336G=
|
|
ENST00000579204.1:c.447G=
|
ENSP00000464629.1:n.447G=
|
|
ENST00000579314.5:c.544G=
|
ENSP00000462599.1:p.Val182=
|
|
ENST00000579726.5:c.828G=
|
|
|
ENST00000582005.5:c.*186G=
|
ENSP00000462002.1:n.*186G=
|
|
ENST00000582761.1:c.34G=
|
ENSP00000462909.1:p.Val12=
|
|
ENST00000584865.5:n.212G=
|
|
|
NM_000789.3:c.2266G=
|
NP_000780.1:p.Val756=
|
|
NM_001178057.1:c.544G=
|
NP_001171528.1:p.Val182=
|
|
NM_152830.2:c.544G=
|
NP_690043.1:p.Val182=
|
|
XM_005257110.1:c.1717G=
|
XP_005257167.1:p.Val573=
|
|
XM_006721737.2:c.604G=
|
XP_006721800.2:p.Val202=
|
|
XM_006721737.3:c.604G=
|
XP_006721800.2:p.Val202=
|
|
NM_000789.4:c.2266G=
MANE Select
|
NP_000780.1:p.Val756=
|
|
NM_001178057.2:c.544G=
|
NP_001171528.1:p.Val182=
|
|
NM_152830.3:c.544G=
|
NP_690043.1:p.Val182=
|
|
NM_001382700.1:c.1699G=
|
NP_001369629.1:p.Val567=
|
|
NM_001382701.1:c.1414G=
|
NP_001369630.1:p.Val472=
|
|
NM_001382702.1:c.196G=
|
NP_001369631.1:p.Val66=
|
|
NR_168483.1:n.566G=
|
|
|