ENST00000478003.2:n.2290A>T
|
|
|
ENST00000682103.1:c.3A>T
|
|
|
ENST00000682276.1:n.1907A>T
|
|
|
ENST00000682892.1:c.2009A>T
|
ENSP00000507214.1:p.Glu670Val
|
|
ENST00000682952.1:n.2101A>T
|
|
|
ENST00000684455.1:c.1675A>T
|
|
|
ENST00000684642.1:c.1859A>T
|
ENSP00000507355.1:p.Glu620Val
|
|
ENST00000684740.1:n.2640A>T
|
|
|
ENST00000303236.9:c.2462A>T
MANE Select
|
ENSP00000307235.3:p.Glu821Val
|
|
ENST00000652099.1:c.2656A>T
|
|
|
ENST00000652736.1:n.2338A>T
|
|
|
ENST00000303236.7:c.2462A>T
|
ENSP00000307235.3:p.Glu821Val
|
|
ENST00000415570.1:c.2099A>T
|
ENSP00000412076.1:p.Glu700Val
|
|
ENST00000419748.5:c.2009A>T
|
ENSP00000408325.1:p.Glu670Val
|
|
ENST00000470706.1:n.105A>T
|
|
|
NM_001313915.1:c.2009A>T
|
NP_001300844.1:p.Glu670Val
|
|
NM_004836.5:c.2462A>T
|
NP_004827.4:p.Glu821Val
|
|
NM_004836.6:c.2462A>T
|
NP_004827.4:p.Glu821Val
|
|
NR_110236.1:n.1158T>A
|
|
|
XM_005264649.3:c.1778A>T
|
XP_005264706.1:p.Glu593Val
|
|
XM_017005376.2:c.1778A>T
|
XP_016860865.1:p.Glu593Val
|
|
NM_004836.7:c.2462A>T
MANE Select
|
NP_004827.4:p.Glu821Val
|
|
NM_001313915.2:c.2009A>T
|
NP_001300844.1:p.Glu670Val
|
|