|
NM_004514.4:c.154C>T
MANE Select
|
NP_004505.2:p.Arg52Cys
|
|
ENST00000335255.10:c.154C>T
MANE Select
|
ENSP00000335677.5:p.Arg52Cys
|
|
NM_004514.3:c.154C>T
|
NP_004505.2:p.Arg52Cys
|
|
ENST00000335255.9:c.154C>T
|
ENSP00000335677.5:p.Arg52Cys
|
|
ENST00000473637.6:c.154C>T
|
ENSP00000436108.2:p.Arg52Cys
|
|
ENST00000527313.6:n.66C>T
|
|
|
ENST00000622867.4:c.143C>T
|
ENSP00000481132.1:p.Ala48Val
|
|
XM_011523573.1:c.154C>T
|
XP_011521875.1:p.Arg52Cys
|
|
XM_024450739.1:c.-515C>T
|
XP_024306507.1:n.-515C>T
|
|
XR_001752506.1:n.273C>T
|
|
|
XR_933935.1:n.210C>T
|
|
|
XR_933935.2:n.273C>T
|
|