ENST00000260408.8:c.1509C>T
MANE Select
|
ENSP00000260408.3:p.Cys503=
|
|
ENST00000260408.7:c.1509C>T
|
ENSP00000260408.3:p.Cys503=
|
|
ENST00000396136.6:c.1335C>T
|
|
|
ENST00000402627.5:c.154+11842C>T
|
ENSP00000386056.1:n.154+11842C>T
|
|
ENST00000462061.1:n.69C>T
|
|
|
ENST00000470269.5:n.38C>T
|
|
|
ENST00000475898.1:n.534C>T
|
|
|
ENST00000481164.1:n.32C>T
|
|
|
ENST00000482945.5:n.32C>T
|
|
|
ENST00000561288.1:c.56-23955C>T
|
ENSP00000452639.1:n.56-23955C>T
|
|
NM_001110.3:c.1509C>T
|
NP_001101.1:p.Cys503=
|
|
XM_005254117.2:c.1416C>T
|
XP_005254174.1:p.Cys472=
|
|
NM_001320570.1:c.1416C>T
|
NP_001307499.1:p.Cys472=
|
|
XM_024449818.1:c.1287C>T
|
XP_024305586.1:p.Cys429=
|
|
NM_001110.4:c.1509C>T
MANE Select
|
NP_001101.1:p.Cys503=
|
|
NM_001320570.2:c.1416C>T
|
NP_001307499.1:p.Cys472=
|
|