ENST00000260408.8:c.1511G=
MANE Select
|
ENSP00000260408.3:p.Ser504=
|
|
ENST00000260408.7:c.1511G=
|
ENSP00000260408.3:p.Ser504=
|
|
ENST00000396136.6:c.1337G=
|
|
|
ENST00000402627.5:c.154+11844G=
|
ENSP00000386056.1:n.154+11844G=
|
|
ENST00000462061.1:n.71G=
|
|
|
ENST00000470269.5:n.40G=
|
|
|
ENST00000475898.1:n.536G=
|
|
|
ENST00000481164.1:n.34G=
|
|
|
ENST00000482945.5:n.34G=
|
|
|
ENST00000561288.1:c.56-23953G=
|
ENSP00000452639.1:n.56-23953G=
|
|
NM_001110.3:c.1511G=
|
NP_001101.1:p.Ser504=
|
|
XM_005254117.2:c.1418G=
|
XP_005254174.1:p.Ser473=
|
|
NM_001320570.1:c.1418G=
|
NP_001307499.1:p.Ser473=
|
|
XM_024449818.1:c.1289G=
|
XP_024305586.1:p.Ser430=
|
|
NM_001110.4:c.1511G=
MANE Select
|
NP_001101.1:p.Ser504=
|
|
NM_001320570.2:c.1418G=
|
NP_001307499.1:p.Ser473=
|
|