|
NM_000023.4:c.602G>A
MANE Select
|
NP_000014.1:p.Gly201Asp
|
|
ENST00000262018.8:c.602G>A
MANE Select
|
ENSP00000262018.3:p.Gly201Asp
|
|
NM_000023.2:c.602G>A , LRG_203t1:c.602G>A
|
NP_000014.1:p.Gly201Asp
|
|
NM_000023.3:c.602G>A
|
NP_000014.1:p.Gly201Asp
|
|
NM_001135697.1:c.584+537G>A
|
NP_001129169.1:n.584+537G>A
|
|
NM_001135697.2:c.584+537G>A
|
NP_001129169.1:n.584+537G>A
|
|
NM_001135697.3:c.584+537G>A
|
NP_001129169.1:n.584+537G>A
|
|
NR_135553.1:n.658G>A
|
|
|
NR_135553.2:n.638G>A
|
|
|
ENST00000262018.7:c.602G>A
|
ENSP00000262018.3:p.Gly201Asp
|
|
ENST00000344627.10:c.584+537G>A
|
ENSP00000345522.6:n.584+537G>A
|
|
ENST00000502555.5:c.*261G>A
|
ENSP00000422817.1:n.*261G>A
|
|
ENST00000504073.1:c.64+5G>A
|
|
|
ENST00000504073.2:c.597+5G>A
|
ENSP00000422030.2:n.597+5G>A
|
|
ENST00000511303.5:c.305+537G>A
|
ENSP00000426104.1:n.305+537G>A
|
|
ENST00000511303.6:n.309+537G>A
|
|
|
ENST00000512526.1:c.419+537G>A
|
|
|
ENST00000512526.2:c.575+537G>A
|
ENSP00000426606.2:n.575+537G>A
|
|
ENST00000513821.5:c.602G>A
|
ENSP00000426571.1:p.Gly201Asp
|
|
ENST00000513942.5:n.375+537G>A
|
|
|
ENST00000682109.1:c.482G>A
|
ENSP00000508041.1:p.Gly161Asp
|
|
ENST00000683226.1:n.312G>A
|
|
|
ENST00000683294.1:c.602G>A
|
ENSP00000508134.1:p.Gly201Asp
|
|
XM_011525120.1:c.602G>A
|
XP_011523422.1:p.Gly201Asp
|
|
XM_011525120.2:c.764G>A
|
XP_011523422.2:p.Gly255Asp
|
|
XM_011525121.1:c.597+5G>A
|
XP_011523423.1:n.597+5G>A
|
|
XM_011525121.2:c.759+5G>A
|
XP_011523423.2:n.759+5G>A
|
|
XM_011525122.1:c.602G>A
|
XP_011523424.1:p.Gly201Asp
|
|
XM_011525122.2:c.764G>A
|
XP_011523424.2:p.Gly255Asp
|
|
XM_011525123.1:c.584+537G>A
|
XP_011523425.1:n.584+537G>A
|
|
XM_011525123.2:c.746+537G>A
|
XP_011523425.2:n.746+537G>A
|
|
XM_011525124.1:c.296G>A
|
XP_011523426.1:p.Gly99Asp
|
|
XM_011525124.2:c.296G>A
|
XP_011523426.1:p.Gly99Asp
|
|
XM_024450873.1:c.296G>A
|
XP_024306641.1:p.Gly99Asp
|
|
XR_002958056.1:n.1120G>A
|
|
|
XR_934517.1:n.668G>A
|
|
