ENST00000399503.4:c.795A>G
MANE Select
|
ENSP00000382423.3:p.Glu265=
|
|
ENST00000399503.3:c.795A>G
|
ENSP00000382423.3:p.Glu265=
|
|
NM_005921.1:c.795A>G
|
NP_005912.1:p.Glu265=
|
|
XM_005248519.3:c.417A>G
|
XP_005248576.2:p.Glu139=
|
|
XM_011543406.1:c.540A>G
|
XP_011541708.1:p.Glu180=
|
|
XM_011543407.1:c.795A>G
|
XP_011541709.1:p.Glu265=
|
|
XM_011543408.1:c.795A>G
|
XP_011541710.1:p.Glu265=
|
|
XM_017009484.1:c.384A>G
|
XP_016864973.1:p.Glu128=
|
|
XM_017009485.1:c.306A>G
|
XP_016864974.1:p.Glu102=
|
|
XR_001742068.2:n.826A>G
|
|
|
NM_005921.2:c.795A>G
MANE Select
|
NP_005912.1:p.Glu265=
|
|