ENST00000260408.8:c.515G=
MANE Select
|
ENSP00000260408.3:p.Gly172=
|
|
ENST00000260408.7:c.515G=
|
ENSP00000260408.3:p.Gly172=
|
|
ENST00000396136.6:c.341G=
|
|
|
ENST00000402627.5:c.56-24337G=
|
ENSP00000386056.1:n.56-24337G=
|
|
ENST00000439637.5:c.356G=
|
ENSP00000391930.1:p.Gly119=
|
|
ENST00000497846.5:n.632G=
|
|
|
ENST00000558733.5:n.751G=
|
|
|
ENST00000559053.1:c.56-24337G=
|
ENSP00000453952.1:n.56-24337G=
|
|
ENST00000561288.1:c.56-67649G=
|
ENSP00000452639.1:n.56-67649G=
|
|
NM_001110.3:c.515G=
|
NP_001101.1:p.Gly172=
|
|
XM_005254117.2:c.515G=
|
XP_005254174.1:p.Gly172=
|
|
NM_001320570.1:c.515G=
|
NP_001307499.1:p.Gly172=
|
|
XM_024449818.1:c.293G=
|
XP_024305586.1:p.Gly98=
|
|
NM_001110.4:c.515G=
MANE Select
|
NP_001101.1:p.Gly172=
|
|
NM_001320570.2:c.515G=
|
NP_001307499.1:p.Gly172=
|
|