ENST00000478003.2:n.2054A>C
|
|
|
ENST00000682276.1:n.1671A>C
|
|
|
ENST00000682892.1:c.1773A>C
|
ENSP00000507214.1:p.Glu591Asp
|
|
ENST00000682952.1:n.1865A>C
|
|
|
ENST00000684455.1:c.1439A>C
|
|
|
ENST00000684642.1:c.1623A>C
|
ENSP00000507355.1:p.Glu541Asp
|
|
ENST00000684740.1:n.2404A>C
|
|
|
ENST00000303236.9:c.2226A>C
MANE Select
|
ENSP00000307235.3:p.Glu742Asp
|
|
ENST00000652099.1:c.2420A>C
|
|
|
ENST00000652736.1:n.2102A>C
|
|
|
ENST00000303236.7:c.2226A>C
|
ENSP00000307235.3:p.Glu742Asp
|
|
ENST00000415570.1:c.1863A>C
|
ENSP00000412076.1:p.Glu621Asp
|
|
ENST00000419748.5:c.1773A>C
|
ENSP00000408325.1:p.Glu591Asp
|
|
ENST00000470706.1:n.48+104A>C
|
|
|
NM_001313915.1:c.1773A>C
|
NP_001300844.1:p.Glu591Asp
|
|
NM_004836.5:c.2226A>C
|
NP_004827.4:p.Glu742Asp
|
|
NM_004836.6:c.2226A>C
|
NP_004827.4:p.Glu742Asp
|
|
NR_110236.1:n.1394T>G
|
|
|
XM_005264649.3:c.1542A>C
|
XP_005264706.1:p.Glu514Asp
|
|
XM_017005376.2:c.1542A>C
|
XP_016860865.1:p.Glu514Asp
|
|
NM_004836.7:c.2226A>C
MANE Select
|
NP_004827.4:p.Glu742Asp
|
|
NM_001313915.2:c.1773A>C
|
NP_001300844.1:p.Glu591Asp
|
|