|
NM_001002295.2:c.990G>A
MANE Select
|
NP_001002295.1:p.Arg330=
|
|
ENST00000379328.9:c.990G>A
MANE Select
|
ENSP00000368632.3:p.Arg330=
|
|
NM_001002295.1:c.990G>A
|
NP_001002295.1:p.Arg330=
|
|
NM_002051.2:c.987G>A
|
NP_002042.1:p.Arg329=
|
|
NM_002051.3:c.987G>A
|
NP_002042.1:p.Arg329=
|
|
ENST00000346208.3:c.987G>A
|
ENSP00000341619.3:p.Arg329=
|
|
ENST00000346208.4:c.987G>A
|
ENSP00000341619.3:p.Arg329=
|
|
ENST00000379328.7:c.990G>A
|
ENSP00000368632.3:p.Arg330=
|
|
ENST00000461472.1:n.509G>A
|
|
|
XM_005252442.2:c.990G>A
|
XP_005252499.1:p.Arg330=
|
|
XM_005252443.3:c.990G>A
|
XP_005252500.1:p.Arg330=
|
|
XM_005252443.5:c.990G>A
|
XP_005252500.1:p.Arg330=
|