ENST00000379370.7:c.2075G>T
MANE Select
|
ENSP00000368678.2:p.Gly692Val
|
|
ENST00000651234.1:c.1760G>T
|
ENSP00000499046.1:p.Gly587Val
|
|
ENST00000652369.1:c.1760G>T
|
ENSP00000498543.1:p.Gly587Val
|
|
ENST00000379370.6:c.2075G>T
|
ENSP00000368678.2:p.Gly692Val
|
|
ENST00000620552.4:c.1661G>T
|
ENSP00000484607.1:p.Gly554Val
|
|
NM_001305275.1:c.2075G>T
|
NP_001292204.1:p.Gly692Val
|
|
NM_198576.3:c.2075G>T
|
NP_940978.2:p.Gly692Val
|
|
XM_005244749.2:c.2075G>T
|
XP_005244806.1:p.Gly692Val
|
|
XM_006710635.2:c.2075G>T
|
XP_006710698.1:p.Gly692Val
|
|
XM_011541429.1:c.2075G>T
|
XP_011539731.1:p.Gly692Val
|
|
XM_011541430.1:c.1202G>T
|
XP_011539732.1:p.Gly401Val
|
|
XM_011541431.1:c.341G>T
|
XP_011539733.1:p.Gly114Val
|
|
XR_946650.1:n.2142G>T
|
|
|
NM_001364727.1:c.1760G>T
|
NP_001351656.1:p.Gly587Val
|
|
XM_005244749.3:c.2075G>T
|
XP_005244806.1:p.Gly692Val
|
|
XM_011541429.2:c.2075G>T
|
XP_011539731.1:p.Gly692Val
|
|
XR_946650.2:n.2146G>T
|
|
|
NM_001305275.2:c.2075G>T
|
NP_001292204.1:p.Gly692Val
|
|
NM_198576.4:c.2075G>T
MANE Select
|
NP_940978.2:p.Gly692Val
|
|
NM_001364727.2:c.1760G>T
|
NP_001351656.1:p.Gly587Val
|
|