ENST00000396705.10:c.694G=
MANE Select
|
ENSP00000379933.4:p.Val232=
|
|
ENST00000229270.8:c.805G=
|
ENSP00000229270.4:p.Val269=
|
|
ENST00000396705.9:c.694G=
|
ENSP00000379933.4:p.Val232=
|
|
ENST00000474253.1:n.183G=
|
|
|
ENST00000488464.6:c.448G=
|
ENSP00000475620.1:p.Val150=
|
|
ENST00000535434.5:c.448G=
|
ENSP00000443599.1:p.Val150=
|
|
ENST00000613953.4:c.805G=
|
ENSP00000484435.1:p.Val269=
|
|
NM_000365.5:c.694G=
|
NP_000356.1:p.Val232=
|
|
NM_001159287.1:c.805G=
|
NP_001152759.1:p.Val269=
|
|
NM_001258026.1:c.448G=
|
NP_001244955.1:p.Val150=
|
|
XR_002957378.1:n.1702G=
|
|
|
NM_000365.6:c.694G=
MANE Select
|
NP_000356.1:p.Val232=
|
|
NM_001258026.2:c.448G=
|
NP_001244955.1:p.Val150=
|
|