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NM_144701.3:c.1867A>G
MANE Select
|
NP_653302.2:p.Arg623Gly
|
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ENST00000347310.10:c.1867A>G
MANE Select
|
ENSP00000321345.5:p.Arg623Gly
|
|
NM_144701.2:c.1867A>G
|
NP_653302.2:p.Arg623Gly
|
|
ENST00000347310.9:c.1867A>G
|
ENSP00000321345.5:p.Arg623Gly
|
|
ENST00000395227.2:c.661A>G
|
ENSP00000378652.2:p.Arg221Gly
|
|
ENST00000425614.3:c.1102A>G
|
ENSP00000387640.2:p.Arg368Gly
|
|
ENST00000473881.2:c.*693A>G
|
ENSP00000486667.1:n.*693A>G
|
|
ENST00000637002.1:c.1258A>G
|
ENSP00000490340.1:p.Arg420Gly
|
|
ENST00000697149.1:c.1706A>G
|
ENSP00000513138.1:n.1706A>G
|
|
ENST00000697150.1:c.1764A>G
|
ENSP00000513139.1:n.1764A>G
|
|
ENST00000697151.1:c.1697A>G
|
ENSP00000513140.1:n.1697A>G
|
|
ENST00000697164.1:c.1777A>G
|
ENSP00000513153.1:p.Arg593Gly
|
|
ENST00000697165.1:c.1564A>G
|
ENSP00000513154.1:p.Arg522Gly
|
|
XM_005270516.2:c.1105A>G
|
XP_005270573.1:p.Arg369Gly
|
|
XM_011540789.1:c.1957A>G
|
XP_011539091.1:p.Arg653Gly
|
|
XM_011540790.1:c.1867A>G
|
XP_011539092.1:p.Arg623Gly
|
|
XM_011540790.3:c.1867A>G
|
XP_011539092.1:p.Arg623Gly
|
|
XM_011540791.1:c.1867A>G
|
XP_011539093.1:p.Arg623Gly
|
|
XM_011540791.3:c.1867A>G
|
XP_011539093.1:p.Arg623Gly
|
|
XR_001736993.1:n.1947A>G
|
|