ENST00000368985.8:c.931C>G
MANE Select
|
ENSP00000357981.3:p.Arg311Gly
|
|
ENST00000448301.7:c.703C>G
|
ENSP00000408414.2:p.Arg235Gly
|
|
ENST00000472977.7:c.931C>G
|
ENSP00000475176.2:p.Arg311Gly
|
|
ENST00000483930.2:c.*125C>G
|
ENSP00000475812.2:n.*125C>G
|
|
ENST00000607427.2:c.931C>G
|
ENSP00000475557.2:p.Arg311Gly
|
|
ENST00000679512.1:c.828C>G
|
ENSP00000505113.1:p.Phe276Leu
|
|
ENST00000679898.1:c.658C>G
|
ENSP00000505326.1:p.Arg220Gly
|
|
ENST00000680288.1:c.781C>G
|
ENSP00000506001.1:p.Arg261Gly
|
|
ENST00000680311.1:c.*14C>G
|
ENSP00000505020.1:n.*14C>G
|
|
ENST00000680471.1:c.*102C>G
|
ENSP00000506603.1:n.*102C>G
|
|
ENST00000680664.1:c.754C>G
|
ENSP00000506248.1:p.Arg252Gly
|
|
ENST00000680931.1:c.*281C>G
|
ENSP00000504934.1:n.*281C>G
|
|
ENST00000681357.1:n.321C>G
|
|
|
ENST00000681444.1:c.931C>G
|
ENSP00000505359.1:p.Arg311Gly
|
|
ENST00000368985.7:c.931C>G
|
ENSP00000357981.3:p.Arg311Gly
|
|
ENST00000448301.6:c.781C>G
|
ENSP00000408414.1:p.Arg261Gly
|
|
ENST00000472977.6:c.224C>G
|
|
|
ENST00000483930.1:c.479C>G
|
ENSP00000475812.1:n.479C>G
|
|
NM_001199739.1:c.781C>G
|
NP_001186668.1:p.Arg261Gly
|
|
NM_004079.4:c.931C>G
|
NP_004070.3:p.Arg311Gly
|
|
NM_004079.5:c.931C>G
MANE Select
|
NP_004070.3:p.Arg311Gly
|
|
NM_001199739.2:c.781C>G
|
NP_001186668.1:p.Arg261Gly
|
|