ENST00000478003.2:n.1912T>A
|
|
|
ENST00000682276.1:n.1529T>A
|
|
|
ENST00000682892.1:c.1631T>A
|
ENSP00000507214.1:p.Val544Asp
|
|
ENST00000682952.1:n.1723T>A
|
|
|
ENST00000684455.1:c.1297T>A
|
|
|
ENST00000684642.1:c.1481T>A
|
ENSP00000507355.1:p.Val494Asp
|
|
ENST00000684740.1:n.2262T>A
|
|
|
ENST00000303236.9:c.2084T>A
MANE Select
|
ENSP00000307235.3:p.Val695Asp
|
|
ENST00000652099.1:c.2278T>A
|
|
|
ENST00000652736.1:n.1960T>A
|
|
|
ENST00000303236.7:c.2084T>A
|
ENSP00000307235.3:p.Val695Asp
|
|
ENST00000415570.1:c.1721T>A
|
ENSP00000412076.1:p.Val574Asp
|
|
ENST00000419748.5:c.1631T>A
|
ENSP00000408325.1:p.Val544Asp
|
|
ENST00000470706.1:n.10T>A
|
|
|
ENST00000478003.1:n.650T>A
|
|
|
NM_001313915.1:c.1631T>A
|
NP_001300844.1:p.Val544Asp
|
|
NM_004836.5:c.2084T>A
|
NP_004827.4:p.Val695Asp
|
|
NM_004836.6:c.2084T>A
|
NP_004827.4:p.Val695Asp
|
|
NR_110236.1:n.1536A>T
|
|
|
XM_005264649.3:c.1400T>A
|
XP_005264706.1:p.Val467Asp
|
|
XR_939749.1:n.2363T>A
|
|
|
XM_017005376.2:c.1400T>A
|
XP_016860865.1:p.Val467Asp
|
|
NM_004836.7:c.2084T>A
MANE Select
|
NP_004827.4:p.Val695Asp
|
|
NM_001313915.2:c.1631T>A
|
NP_001300844.1:p.Val544Asp
|
|