ENST00000713569.1:c.928G>A
|
ENSP00000518862.1:p.Glu310Lys
|
|
ENST00000280346.11:c.928G>A
MANE Select
|
ENSP00000280346.7:p.Glu310Lys
|
|
ENST00000527231.2:n.975G>A
|
|
|
ENST00000531306.2:c.547G>A
|
ENSP00000433432.2:p.Glu183Lys
|
|
ENST00000679368.1:c.788-1831G>A
|
ENSP00000505314.1:n.788-1831G>A
|
|
ENST00000679466.1:n.975G>A
|
|
|
ENST00000679614.1:c.325G>A
|
ENSP00000506007.1:p.Glu109Lys
|
|
ENST00000679815.1:c.*361G>A
|
ENSP00000504880.1:n.*361G>A
|
|
ENST00000679829.1:n.1055G>A
|
|
|
ENST00000679878.1:c.895G>A
|
ENSP00000505567.1:p.Glu299Lys
|
|
ENST00000680010.1:c.*69G>A
|
ENSP00000505768.1:n.*69G>A
|
|
ENST00000680331.1:c.649G>A
|
ENSP00000506707.1:p.Glu217Lys
|
|
ENST00000680411.1:c.673G>A
|
ENSP00000505915.1:p.Glu225Lys
|
|
ENST00000681316.1:c.928G>A
|
ENSP00000506560.1:p.Glu310Lys
|
|
ENST00000681328.1:c.928G>A
|
ENSP00000506355.1:p.Glu310Lys
|
|
ENST00000681339.1:c.928G>A
|
ENSP00000506167.1:p.Glu310Lys
|
|
ENST00000681638.1:c.*281G>A
|
ENSP00000506090.1:n.*281G>A
|
|
ENST00000280346.10:c.928G>A
|
ENSP00000280346.6:p.Glu310Lys
|
|
ENST00000393051.5:c.661-1831G>A
|
ENSP00000376771.1:n.661-1831G>A
|
|
ENST00000531306.1:c.424G>A
|
ENSP00000433432.1:p.Glu142Lys
|
|
ENST00000533297.1:c.*603G>A
|
ENSP00000435374.1:n.*603G>A
|
|
NM_001931.4:c.928G>A
|
NP_001922.2:p.Glu310Lys
|
|
XM_011542647.1:c.928G>A
|
XP_011540949.1:p.Glu310Lys
|
|
XM_011542647.3:c.928G>A
|
XP_011540949.1:p.Glu310Lys
|
|
NM_001372031.1:c.928G>A
|
NP_001358960.1:p.Glu310Lys
|
|
NM_001372032.1:c.928G>A
|
NP_001358961.1:p.Glu310Lys
|
|
NM_001372033.1:c.928G>A
|
NP_001358962.1:p.Glu310Lys
|
|
NM_001372034.1:c.895G>A
|
NP_001358963.1:p.Glu299Lys
|
|
NM_001372035.1:c.928G>A
|
NP_001358964.1:p.Glu310Lys
|
|
NM_001372036.1:c.802G>A
|
NP_001358965.1:p.Glu268Lys
|
|
NM_001372037.1:c.760G>A
|
NP_001358966.1:p.Glu254Lys
|
|
NM_001372038.1:c.649G>A
|
NP_001358967.1:p.Glu217Lys
|
|
NM_001372039.1:c.661-1831G>A
|
NP_001358968.1:n.661-1831G>A
|
|
NM_001372040.1:c.547G>A
|
NP_001358969.1:p.Glu183Lys
|
|
NM_001372041.1:c.661-1831G>A
|
NP_001358970.1:n.661-1831G>A
|
|
NM_001372042.1:c.466G>A
|
NP_001358971.1:p.Glu156Lys
|
|
NM_001931.5:c.928G>A
MANE Select
|
NP_001922.2:p.Glu310Lys
|
|
NR_164072.1:n.853-1831G>A
|
|
|