ENST00000261978.9:c.4697G>C
MANE Select
|
ENSP00000261978.4:p.Cys1566Ser
|
|
ENST00000261978.8:c.4697G>C
|
ENSP00000261978.4:p.Cys1566Ser
|
|
ENST00000553939.5:c.4697G>C
|
ENSP00000452110.1:p.Cys1566Ser
|
|
ENST00000556690.5:c.4565G>C
|
ENSP00000451477.1:p.Cys1522Ser
|
|
NM_000428.2:c.4697G>C
|
NP_000419.1:p.Cys1566Ser
|
|
XM_011536765.1:c.4316G>C
|
XP_011535067.1:p.Cys1439Ser
|
|
XM_011536766.1:c.4238G>C
|
XP_011535068.1:p.Cys1413Ser
|
|
XM_011536767.1:c.4214G>C
|
XP_011535069.1:p.Cys1405Ser
|
|
XM_011536765.2:c.4316G>C
|
XP_011535067.1:p.Cys1439Ser
|
|
NM_000428.3:c.4697G>C
MANE Select
|
NP_000419.1:p.Cys1566Ser
|
|