ENST00000478003.2:n.1900A>T
|
|
|
ENST00000682276.1:n.1517A>T
|
|
|
ENST00000682892.1:c.1619A>T
|
ENSP00000507214.1:p.Asp540Val
|
|
ENST00000682952.1:n.1711A>T
|
|
|
ENST00000684455.1:c.1285A>T
|
|
|
ENST00000684642.1:c.1469A>T
|
ENSP00000507355.1:p.Asp490Val
|
|
ENST00000684740.1:n.2250A>T
|
|
|
ENST00000303236.9:c.2072A>T
MANE Select
|
ENSP00000307235.3:p.Asp691Val
|
|
ENST00000652099.1:c.2266A>T
|
|
|
ENST00000652736.1:n.1948A>T
|
|
|
ENST00000303236.7:c.2072A>T
|
ENSP00000307235.3:p.Asp691Val
|
|
ENST00000415570.1:c.1709A>T
|
ENSP00000412076.1:p.Asp570Val
|
|
ENST00000419748.5:c.1619A>T
|
ENSP00000408325.1:p.Asp540Val
|
|
ENST00000478003.1:n.638A>T
|
|
|
NM_001313915.1:c.1619A>T
|
NP_001300844.1:p.Asp540Val
|
|
NM_004836.5:c.2072A>T
|
NP_004827.4:p.Asp691Val
|
|
NM_004836.6:c.2072A>T
|
NP_004827.4:p.Asp691Val
|
|
NR_110236.1:n.1548T>A
|
|
|
XM_005264649.3:c.1388A>T
|
XP_005264706.1:p.Asp463Val
|
|
XR_939749.1:n.2351A>T
|
|
|
XM_017005376.2:c.1388A>T
|
XP_016860865.1:p.Asp463Val
|
|
NM_004836.7:c.2072A>T
MANE Select
|
NP_004827.4:p.Asp691Val
|
|
NM_001313915.2:c.1619A>T
|
NP_001300844.1:p.Asp540Val
|
|