ENST00000554809.6:c.2762A>G
|
ENSP00000450632.2:p.Glu921Gly
|
|
ENST00000555484.2:c.328A>G
|
|
|
ENST00000556250.6:c.4343A>G
|
ENSP00000452033.2:p.Glu1448Gly
|
|
ENST00000557110.2:c.328A>G
|
|
|
ENST00000696642.1:c.*3361A>G
|
ENSP00000512775.1:n.*3361A>G
|
|
ENST00000696644.1:n.286A>G
|
|
|
ENST00000696645.1:n.440A>G
|
|
|
ENST00000696647.1:c.4550A>G
|
ENSP00000512778.1:p.Glu1517Gly
|
|
ENST00000696648.1:c.*2575A>G
|
ENSP00000512779.1:n.*2575A>G
|
|
ENST00000696649.1:c.4394A>G
|
ENSP00000512780.1:p.Glu1465Gly
|
|
ENST00000696650.1:n.4498A>G
|
|
|
ENST00000696659.1:c.2548A>G
|
|
|
ENST00000696663.1:c.3481A>G
|
|
|
ENST00000696664.1:c.3382A>G
|
|
|
ENST00000696665.1:c.328A>G
|
|
|
ENST00000696675.1:c.*306A>G
|
ENSP00000512799.1:n.*306A>G
|
|
ENST00000696683.1:c.3367A>G
|
|
|
ENST00000696684.1:c.3367A>G
|
|
|
ENST00000696685.1:c.3367A>G
|
|
|
ENST00000696686.1:n.1287A>G
|
|
|
ENST00000267430.10:c.4550A>G
MANE Select
|
ENSP00000267430.5:p.Glu1517Gly
|
|
ENST00000267430.9:c.4550A>G
|
ENSP00000267430.5:p.Glu1517Gly
|
|
ENST00000542564.6:c.4472A>G
|
ENSP00000442493.2:p.Glu1491Gly
|
|
ENST00000554809.5:c.1347A>G
|
|
|
ENST00000555013.1:n.383A>G
|
|
|
ENST00000556250.5:c.3098A>G
|
ENSP00000452033.1:p.Glu1033Gly
|
|
NM_001308133.1:c.4472A>G
|
NP_001295062.1:p.Glu1491Gly
|
|
NM_020937.2:c.4550A>G , LRG_502t1:c.4550A>G
|
NP_065988.1:p.Glu1517Gly
|
|
NM_020937.3:c.4550A>G
|
NP_065988.1:p.Glu1517Gly
|
|
XM_011537034.1:c.4565A>G
|
XP_011535336.1:p.Glu1522Gly
|
|
XM_011537035.1:c.4487A>G
|
XP_011535337.1:p.Glu1496Gly
|
|
XM_011537036.1:c.4565A>G
|
XP_011535338.1:p.Glu1522Gly
|
|
XM_011537037.1:c.2579A>G
|
XP_011535339.1:p.Glu860Gly
|
|
XM_011537034.2:c.4565A>G
|
XP_011535336.1:p.Glu1522Gly
|
|
XM_011537035.3:c.4487A>G
|
XP_011535337.1:p.Glu1496Gly
|
|
XM_011537037.3:c.2579A>G
|
XP_011535339.1:p.Glu860Gly
|
|
XM_017021523.1:c.4565A>G
|
XP_016877012.1:p.Glu1522Gly
|
|
XM_017021524.2:c.3602A>G
|
XP_016877013.1:p.Glu1201Gly
|
|
XM_017021525.2:c.3380A>G
|
XP_016877014.1:p.Glu1127Gly
|
|
XM_017021526.2:c.3380A>G
|
XP_016877015.1:p.Glu1127Gly
|
|
XM_017021527.1:c.3365A>G
|
XP_016877016.1:p.Glu1122Gly
|
|
XR_001750470.1:n.4657A>G
|
|
|
XR_001750471.2:n.4642A>G
|
|
|
XR_001750472.1:n.4694A>G
|
|
|
NM_020937.4:c.4550A>G
MANE Select
|
NP_065988.1:p.Glu1517Gly
|
|
NM_001308133.2:c.4472A>G
|
NP_001295062.1:p.Glu1491Gly
|
|