ENST00000366672.5:c.285G>A
MANE Select
|
ENSP00000355632.4:p.Gly95=
|
|
ENST00000366672.4:c.285G>A
|
ENSP00000355632.4:p.Gly95=
|
|
ENST00000494106.1:n.248G>A
|
|
|
NM_001291866.1:c.171G>A
|
NP_001278795.1:p.Gly57=
|
|
NM_004481.4:c.285G>A
|
NP_004472.1:p.Gly95=
|
|
XM_011544154.1:c.213G>A
|
XP_011542456.1:p.Gly71=
|
|
XM_011544155.1:c.84G>A
|
XP_011542457.1:p.Gly28=
|
|
XM_017000963.2:c.285G>A
|
XP_016856452.1:p.Gly95=
|
|
XM_017000964.2:c.192G>A
|
XP_016856453.1:p.Gly64=
|
|
XM_017000965.1:c.171G>A
|
XP_016856454.1:p.Gly57=
|
|
XM_017000966.1:c.84G>A
|
XP_016856455.1:p.Gly28=
|
|
NM_004481.5:c.285G>A
MANE Select
|
NP_004472.1:p.Gly95=
|
|
NM_001291866.2:c.171G>A
|
NP_001278795.1:p.Gly57=
|
|