ENST00000478003.2:n.2074A>G
|
|
|
ENST00000682276.1:n.1691A>G
|
|
|
ENST00000682892.1:c.1793A>G
|
ENSP00000507214.1:p.Glu598Gly
|
|
ENST00000682952.1:n.1885A>G
|
|
|
ENST00000684455.1:c.1459A>G
|
|
|
ENST00000684642.1:c.1643A>G
|
ENSP00000507355.1:p.Glu548Gly
|
|
ENST00000684740.1:n.2424A>G
|
|
|
ENST00000303236.9:c.2246A>G
MANE Select
|
ENSP00000307235.3:p.Glu749Gly
|
|
ENST00000652099.1:c.2440A>G
|
|
|
ENST00000652736.1:n.2122A>G
|
|
|
ENST00000303236.7:c.2246A>G
|
ENSP00000307235.3:p.Glu749Gly
|
|
ENST00000415570.1:c.1883A>G
|
ENSP00000412076.1:p.Glu628Gly
|
|
ENST00000419748.5:c.1793A>G
|
ENSP00000408325.1:p.Glu598Gly
|
|
ENST00000470706.1:n.48+124A>G
|
|
|
NM_001313915.1:c.1793A>G
|
NP_001300844.1:p.Glu598Gly
|
|
NM_004836.5:c.2246A>G
|
NP_004827.4:p.Glu749Gly
|
|
NM_004836.6:c.2246A>G
|
NP_004827.4:p.Glu749Gly
|
|
NR_110236.1:n.1374T>C
|
|
|
XM_005264649.3:c.1562A>G
|
XP_005264706.1:p.Glu521Gly
|
|
XM_017005376.2:c.1562A>G
|
XP_016860865.1:p.Glu521Gly
|
|
NM_004836.7:c.2246A>G
MANE Select
|
NP_004827.4:p.Glu749Gly
|
|
NM_001313915.2:c.1793A>G
|
NP_001300844.1:p.Glu598Gly
|
|