|
ENST00000372310.8:c.1526C>G
MANE Select
|
ENSP00000361384.4:p.Ala509Gly
|
|
|
ENST00000673836.1:c.1526C>G
|
ENSP00000501314.1:p.Ala509Gly
|
|
|
ENST00000357730.6:c.1583C>G
|
ENSP00000350362.2:p.Ala528Gly
|
|
|
ENST00000360584.6:c.1745C>G
|
ENSP00000353791.2:p.Ala582Gly
|
|
|
ENST00000372306.7:c.1614C>G
|
ENSP00000361380.3:p.Arg538=
|
|
|
ENST00000372307.7:c.1331C>G
|
ENSP00000361381.3:p.Ala444Gly
|
|
|
ENST00000372310.7:c.1526C>G
|
ENSP00000361384.3:p.Ala509Gly
|
|
|
ENST00000475075.6:c.1193C>G
|
ENSP00000434460.1:p.Ala398Gly
|
|
|
NM_001024845.2:c.1526C>G
|
NP_001020016.1:p.Ala509Gly
|
|
|
NM_001261380.1:c.1538C>G
|
NP_001248309.1:p.Ala513Gly
|
|
|
NM_006934.3:c.1583C>G
|
NP_008865.2:p.Ala528Gly
|
|
|
NM_201649.3:c.1745C>G
|
NP_964012.2:p.Ala582Gly
|
|
|
NR_048548.1:n.1786C>G
|
|
|
|
NR_048549.1:n.1509C>G
|
|
|
|
XM_011542017.1:c.1745C>G
|
XP_011540319.1:p.Ala582Gly
|
|
|
NM_001328626.1:c.1193C>G
|
NP_001315555.1:p.Ala398Gly
|
|
|
NM_001328627.1:c.1463C>G
|
NP_001315556.1:p.Ala488Gly
|
|
|
NM_001328628.1:c.1331C>G
|
NP_001315557.1:p.Ala444Gly
|
|
|
NM_001328629.1:c.1526C>G
|
NP_001315558.1:p.Ala509Gly
|
|
|
NM_001328630.1:c.1193C>G
|
NP_001315559.1:p.Ala398Gly
|
|
|
XM_011542017.2:c.1745C>G
|
XP_011540319.1:p.Ala582Gly
|
|
|
XM_017002152.2:c.1445C>G
|
XP_016857641.1:p.Ala482Gly
|
|
|
XM_017002153.2:c.1412C>G
|
XP_016857642.1:p.Ala471Gly
|
|
|
XM_024449295.1:c.1331C>G
|
XP_024305063.1:p.Ala444Gly
|
|
|
NM_001024845.3:c.1526C>G
MANE Select
|
NP_001020016.1:p.Ala509Gly
|
|
|
NM_001261380.2:c.1538C>G
|
NP_001248309.1:p.Ala513Gly
|
|
|
NM_001328626.2:c.1193C>G
|
NP_001315555.1:p.Ala398Gly
|
|
|
NM_001328630.2:c.1193C>G
|
NP_001315559.1:p.Ala398Gly
|
|
|
NM_006934.4:c.1583C>G
|
NP_008865.2:p.Ala528Gly
|
|
|
NM_201649.4:c.1745C>G
|
NP_964012.2:p.Ala582Gly
|
|
|
NR_048548.2:n.1609C>G
|
|
|
