ENST00000379370.7:c.4704G>T
MANE Select
|
ENSP00000368678.2:p.Glu1568Asp
|
|
ENST00000651234.1:c.4389G>T
|
ENSP00000499046.1:p.Glu1463Asp
|
|
ENST00000652369.1:c.4389G>T
|
ENSP00000498543.1:p.Glu1463Asp
|
|
ENST00000379370.6:c.4704G>T
|
ENSP00000368678.2:p.Glu1568Asp
|
|
ENST00000620552.4:c.4290G>T
|
ENSP00000484607.1:p.Glu1430Asp
|
|
NM_001305275.1:c.4704G>T
|
NP_001292204.1:p.Glu1568Asp
|
|
NM_198576.3:c.4704G>T
|
NP_940978.2:p.Glu1568Asp
|
|
XM_005244749.2:c.4704G>T
|
XP_005244806.1:p.Glu1568Asp
|
|
XM_006710635.2:c.4704G>T
|
XP_006710698.1:p.Glu1568Asp
|
|
XM_011541429.1:c.4704G>T
|
XP_011539731.1:p.Glu1568Asp
|
|
XM_011541430.1:c.3831G>T
|
XP_011539732.1:p.Glu1277Asp
|
|
XM_011541431.1:c.2970G>T
|
XP_011539733.1:p.Glu990Asp
|
|
XR_946650.1:n.4771G>T
|
|
|
NM_001364727.1:c.4389G>T
|
NP_001351656.1:p.Glu1463Asp
|
|
XM_005244749.3:c.4704G>T
|
XP_005244806.1:p.Glu1568Asp
|
|
XM_011541429.2:c.4704G>T
|
XP_011539731.1:p.Glu1568Asp
|
|
XR_946650.2:n.4775G>T
|
|
|
NM_001305275.2:c.4704G>T
|
NP_001292204.1:p.Glu1568Asp
|
|
NM_198576.4:c.4704G>T
MANE Select
|
NP_940978.2:p.Glu1568Asp
|
|
NM_001364727.2:c.4389G>T
|
NP_001351656.1:p.Glu1463Asp
|
|