ENST00000272602.7:c.714G>A
MANE Select
|
ENSP00000272602.2:p.Arg238=
|
|
ENST00000272602.6:c.714G>A
|
ENSP00000272602.2:p.Arg238=
|
|
ENST00000393504.5:c.714G>A
|
ENSP00000377140.1:p.Arg238=
|
|
ENST00000409937.1:c.726G>A
|
ENSP00000386761.1:p.Arg242=
|
|
ENST00000436404.6:c.660G>A
|
ENSP00000410070.2:p.Arg220=
|
|
NM_001079878.1:c.660G>A
|
NP_001073347.1:p.Arg220=
|
|
NM_001298.2:c.714G>A
|
NP_001289.1:p.Arg238=
|
|
XM_006712243.2:c.825G>A
|
XP_006712306.1:p.Arg275=
|
|
XM_011510554.1:c.879G>A
|
XP_011508856.1:p.Arg293=
|
|
XM_011510554.2:c.879G>A
|
XP_011508856.1:p.Arg293=
|
|
NM_001079878.2:c.660G>A
|
NP_001073347.1:p.Arg220=
|
|
NM_001298.3:c.714G>A
MANE Select
|
NP_001289.1:p.Arg238=
|
|