ENST00000322953.9:c.1164G>A
MANE Select
|
ENSP00000320509.4:p.Arg388=
|
|
ENST00000322953.8:c.1164G>A
|
ENSP00000320509.4:p.Arg388=
|
|
ENST00000428908.5:c.765G>A
|
ENSP00000412748.1:p.Arg255=
|
|
ENST00000444316.2:c.1074G>A
|
ENSP00000388817.2:p.Arg358=
|
|
ENST00000504592.5:c.1119G>A
|
ENSP00000421443.1:p.Arg373=
|
|
ENST00000508653.5:c.765G>A
|
ENSP00000422314.1:p.Arg255=
|
|
NM_001083907.2:c.1074G>A
|
NP_001077376.2:p.Arg358=
|
|
NM_001127507.2:c.765G>A
|
NP_001120979.2:p.Arg255=
|
|
NM_017935.4:c.1164G>A
|
NP_060405.4:p.Arg388=
|
|
XM_017008337.2:c.1074G>A
|
XP_016863826.1:p.Arg358=
|
|
NM_017935.5:c.1164G>A
MANE Select
|
NP_060405.5:p.Arg388=
|
|
NM_001083907.3:c.1074G>A
|
NP_001077376.3:p.Arg358=
|
|
NM_001127507.3:c.765G>A
|
NP_001120979.3:p.Arg255=
|
|