ENST00000478003.2:n.1901T>G
|
|
|
ENST00000682276.1:n.1518T>G
|
|
|
ENST00000682892.1:c.1620T>G
|
ENSP00000507214.1:p.Asp540Glu
|
|
ENST00000682952.1:n.1712T>G
|
|
|
ENST00000684455.1:c.1286T>G
|
|
|
ENST00000684642.1:c.1470T>G
|
ENSP00000507355.1:p.Asp490Glu
|
|
ENST00000684740.1:n.2251T>G
|
|
|
ENST00000303236.9:c.2073T>G
MANE Select
|
ENSP00000307235.3:p.Asp691Glu
|
|
ENST00000652099.1:c.2267T>G
|
|
|
ENST00000652736.1:n.1949T>G
|
|
|
ENST00000303236.7:c.2073T>G
|
ENSP00000307235.3:p.Asp691Glu
|
|
ENST00000415570.1:c.1710T>G
|
ENSP00000412076.1:p.Asp570Glu
|
|
ENST00000419748.5:c.1620T>G
|
ENSP00000408325.1:p.Asp540Glu
|
|
ENST00000478003.1:n.639T>G
|
|
|
NM_001313915.1:c.1620T>G
|
NP_001300844.1:p.Asp540Glu
|
|
NM_004836.5:c.2073T>G
|
NP_004827.4:p.Asp691Glu
|
|
NM_004836.6:c.2073T>G
|
NP_004827.4:p.Asp691Glu
|
|
NR_110236.1:n.1547A>C
|
|
|
XM_005264649.3:c.1389T>G
|
XP_005264706.1:p.Asp463Glu
|
|
XR_939749.1:n.2352T>G
|
|
|
XM_017005376.2:c.1389T>G
|
XP_016860865.1:p.Asp463Glu
|
|
NM_004836.7:c.2073T>G
MANE Select
|
NP_004827.4:p.Asp691Glu
|
|
NM_001313915.2:c.1620T>G
|
NP_001300844.1:p.Asp540Glu
|
|