ENST00000474381.2:n.2910A>T
|
|
|
ENST00000481849.6:n.2336A>T
|
|
|
ENST00000497377.6:n.2336A>T
|
|
|
ENST00000640094.2:c.863A>T
|
ENSP00000491275.2:p.Glu288Val
|
|
ENST00000696558.1:c.932A>T
|
ENSP00000512716.1:n.932A>T
|
|
ENST00000696559.1:c.863A>T
|
ENSP00000512717.1:p.Glu288Val
|
|
ENST00000696560.1:c.863A>T
|
ENSP00000512718.1:p.Glu288Val
|
|
ENST00000696561.1:c.863A>T
|
ENSP00000512719.1:p.Glu288Val
|
|
ENST00000696562.1:c.863A>T
|
ENSP00000512720.1:p.Glu288Val
|
|
ENST00000412585.7:c.863A>T
MANE Select
|
ENSP00000399168.2:p.Glu288Val
|
|
ENST00000640094.1:c.56A>T
|
ENSP00000491275.1:p.Glu19Val
|
|
ENST00000412585.6:c.863A>T
|
ENSP00000399168.2:p.Glu288Val
|
|
ENST00000463574.1:n.454A>T
|
|
|
NM_005514.6:c.863A>T
|
NP_005505.2:p.Glu288Val
|
|
XM_011514556.1:c.896A>T
|
XP_011512858.1:p.Glu299Val
|
|
XM_011514557.1:c.863A>T
|
XP_011512859.1:p.Glu288Val
|
|
XR_926175.1:n.1302A>T
|
|
|
NM_005514.7:c.863A>T
|
NP_005505.2:p.Glu288Val
|
|
NM_005514.8:c.863A>T
MANE Select
|
NP_005505.2:p.Glu288Val
|
|