ENST00000379370.7:c.1800G>A
MANE Select
|
ENSP00000368678.2:p.Glu600=
|
|
ENST00000651234.1:c.1485G>A
|
ENSP00000499046.1:p.Glu495=
|
|
ENST00000652369.1:c.1485G>A
|
ENSP00000498543.1:p.Glu495=
|
|
ENST00000379370.6:c.1800G>A
|
ENSP00000368678.2:p.Glu600=
|
|
ENST00000620552.4:c.1386G>A
|
ENSP00000484607.1:p.Glu462=
|
|
NM_001305275.1:c.1800G>A
|
NP_001292204.1:p.Glu600=
|
|
NM_198576.3:c.1800G>A
|
NP_940978.2:p.Glu600=
|
|
XM_005244749.2:c.1800G>A
|
XP_005244806.1:p.Glu600=
|
|
XM_006710635.2:c.1800G>A
|
XP_006710698.1:p.Glu600=
|
|
XM_011541429.1:c.1800G>A
|
XP_011539731.1:p.Glu600=
|
|
XM_011541430.1:c.927G>A
|
XP_011539732.1:p.Glu309=
|
|
XM_011541431.1:c.66G>A
|
XP_011539733.1:p.Glu22=
|
|
XR_946650.1:n.1867G>A
|
|
|
NM_001364727.1:c.1485G>A
|
NP_001351656.1:p.Glu495=
|
|
XM_005244749.3:c.1800G>A
|
XP_005244806.1:p.Glu600=
|
|
XM_011541429.2:c.1800G>A
|
XP_011539731.1:p.Glu600=
|
|
XR_946650.2:n.1871G>A
|
|
|
NM_001305275.2:c.1800G>A
|
NP_001292204.1:p.Glu600=
|
|
NM_198576.4:c.1800G>A
MANE Select
|
NP_940978.2:p.Glu600=
|
|
NM_001364727.2:c.1485G>A
|
NP_001351656.1:p.Glu495=
|
|