ENST00000368985.8:c.940A>G
MANE Select
|
ENSP00000357981.3:p.Arg314Gly
|
|
ENST00000448301.7:c.712A>G
|
ENSP00000408414.2:p.Arg238Gly
|
|
ENST00000472977.7:c.940A>G
|
ENSP00000475176.2:p.Arg314Gly
|
|
ENST00000483930.2:c.*134A>G
|
ENSP00000475812.2:n.*134A>G
|
|
ENST00000607427.2:c.940A>G
|
ENSP00000475557.2:p.Arg314Gly
|
|
ENST00000679512.1:c.837A>G
|
ENSP00000505113.1:p.Gln279=
|
|
ENST00000679898.1:c.667A>G
|
ENSP00000505326.1:p.Arg223Gly
|
|
ENST00000680288.1:c.790A>G
|
ENSP00000506001.1:p.Arg264Gly
|
|
ENST00000680311.1:c.*23A>G
|
ENSP00000505020.1:n.*23A>G
|
|
ENST00000680471.1:c.*111A>G
|
ENSP00000506603.1:n.*111A>G
|
|
ENST00000680664.1:c.763A>G
|
ENSP00000506248.1:p.Arg255Gly
|
|
ENST00000680931.1:c.*290A>G
|
ENSP00000504934.1:n.*290A>G
|
|
ENST00000681357.1:n.330A>G
|
|
|
ENST00000681444.1:c.940A>G
|
ENSP00000505359.1:p.Arg314Gly
|
|
ENST00000368985.7:c.940A>G
|
ENSP00000357981.3:p.Arg314Gly
|
|
ENST00000448301.6:c.790A>G
|
ENSP00000408414.1:p.Arg264Gly
|
|
ENST00000472977.6:c.233A>G
|
|
|
ENST00000483930.1:c.488A>G
|
ENSP00000475812.1:n.488A>G
|
|
NM_001199739.1:c.790A>G
|
NP_001186668.1:p.Arg264Gly
|
|
NM_004079.4:c.940A>G
|
NP_004070.3:p.Arg314Gly
|
|
NM_004079.5:c.940A>G
MANE Select
|
NP_004070.3:p.Arg314Gly
|
|
NM_001199739.2:c.790A>G
|
NP_001186668.1:p.Arg264Gly
|
|