ENST00000322953.9:c.1092A=
MANE Select
|
ENSP00000320509.4:p.Gln364=
|
|
ENST00000322953.8:c.1092A=
|
ENSP00000320509.4:p.Gln364=
|
|
ENST00000428908.5:c.693A=
|
ENSP00000412748.1:p.Gln231=
|
|
ENST00000444316.2:c.1002A=
|
ENSP00000388817.2:p.Gln334=
|
|
ENST00000504592.5:c.1047A=
|
ENSP00000421443.1:p.Gln349=
|
|
ENST00000508653.5:c.693A=
|
ENSP00000422314.1:p.Gln231=
|
|
NM_001083907.2:c.1002A=
|
NP_001077376.2:p.Gln334=
|
|
NM_001127507.2:c.693A=
|
NP_001120979.2:p.Gln231=
|
|
NM_017935.4:c.1092A=
|
NP_060405.4:p.Gln364=
|
|
XM_017008337.2:c.1002A=
|
XP_016863826.1:p.Gln334=
|
|
NM_017935.5:c.1092A=
MANE Select
|
NP_060405.5:p.Gln364=
|
|
NM_001083907.3:c.1002A=
|
NP_001077376.3:p.Gln334=
|
|
NM_001127507.3:c.693A=
|
NP_001120979.3:p.Gln231=
|
|