ENST00000293778.12:c.759T>C
MANE Select
|
ENSP00000293778.7:p.Asn253=
|
|
ENST00000574412.6:c.759T>C
|
ENSP00000459592.2:p.Asn253=
|
|
ENST00000293778.10:c.816T>C
|
ENSP00000293778.6:p.Asn272=
|
|
ENST00000574412.5:c.816T>C
|
ENSP00000459592.1:p.Asn272=
|
|
ENST00000575168.1:n.590T>C
|
|
|
ENST00000576153.5:n.550T>C
|
|
|
NM_001100812.1:c.816T>C
|
NP_001094282.1:p.Asn272=
|
|
NM_022059.3:c.816T>C
|
NP_071342.2:p.Asn272=
|
|
NM_022059.4:c.816T>C
|
NP_071342.2:p.Asn272=
|
|
NM_001100812.2:c.759T>C
|
NP_001094282.2:p.Asn253=
|
|
NM_001386809.1:c.759T>C
MANE Select
|
NP_001373738.1:p.Asn253=
|
|