ENST00000379370.7:c.4855C>G
MANE Select
|
ENSP00000368678.2:p.Arg1619Gly
|
|
ENST00000651234.1:c.4540C>G
|
ENSP00000499046.1:p.Arg1514Gly
|
|
ENST00000652369.1:c.4540C>G
|
ENSP00000498543.1:p.Arg1514Gly
|
|
ENST00000379370.6:c.4855C>G
|
ENSP00000368678.2:p.Arg1619Gly
|
|
ENST00000620552.4:c.4441C>G
|
ENSP00000484607.1:p.Arg1481Gly
|
|
NM_001305275.1:c.4855C>G
|
NP_001292204.1:p.Arg1619Gly
|
|
NM_198576.3:c.4855C>G
|
NP_940978.2:p.Arg1619Gly
|
|
XM_005244749.2:c.4855C>G
|
XP_005244806.1:p.Arg1619Gly
|
|
XM_006710635.2:c.4855C>G
|
XP_006710698.1:p.Arg1619Gly
|
|
XM_011541429.1:c.4855C>G
|
XP_011539731.1:p.Arg1619Gly
|
|
XM_011541430.1:c.3982C>G
|
XP_011539732.1:p.Arg1328Gly
|
|
XM_011541431.1:c.3121C>G
|
XP_011539733.1:p.Arg1041Gly
|
|
XR_946650.1:n.4922C>G
|
|
|
NM_001364727.1:c.4540C>G
|
NP_001351656.1:p.Arg1514Gly
|
|
XM_005244749.3:c.4855C>G
|
XP_005244806.1:p.Arg1619Gly
|
|
XM_011541429.2:c.4855C>G
|
XP_011539731.1:p.Arg1619Gly
|
|
XR_946650.2:n.4926C>G
|
|
|
NM_001305275.2:c.4855C>G
|
NP_001292204.1:p.Arg1619Gly
|
|
NM_198576.4:c.4855C>G
MANE Select
|
NP_940978.2:p.Arg1619Gly
|
|
NM_001364727.2:c.4540C>G
|
NP_001351656.1:p.Arg1514Gly
|
|