ENST00000379370.7:c.1824T>G
MANE Select
|
ENSP00000368678.2:p.Ala608=
|
|
ENST00000651234.1:c.1509T>G
|
ENSP00000499046.1:p.Ala503=
|
|
ENST00000652369.1:c.1509T>G
|
ENSP00000498543.1:p.Ala503=
|
|
ENST00000379370.6:c.1824T>G
|
ENSP00000368678.2:p.Ala608=
|
|
ENST00000620552.4:c.1410T>G
|
ENSP00000484607.1:p.Ala470=
|
|
NM_001305275.1:c.1824T>G
|
NP_001292204.1:p.Ala608=
|
|
NM_198576.3:c.1824T>G
|
NP_940978.2:p.Ala608=
|
|
XM_005244749.2:c.1824T>G
|
XP_005244806.1:p.Ala608=
|
|
XM_006710635.2:c.1824T>G
|
XP_006710698.1:p.Ala608=
|
|
XM_011541429.1:c.1824T>G
|
XP_011539731.1:p.Ala608=
|
|
XM_011541430.1:c.951T>G
|
XP_011539732.1:p.Ala317=
|
|
XM_011541431.1:c.90T>G
|
XP_011539733.1:p.Ala30=
|
|
XR_946650.1:n.1891T>G
|
|
|
NM_001364727.1:c.1509T>G
|
NP_001351656.1:p.Ala503=
|
|
XM_005244749.3:c.1824T>G
|
XP_005244806.1:p.Ala608=
|
|
XM_011541429.2:c.1824T>G
|
XP_011539731.1:p.Ala608=
|
|
XR_946650.2:n.1895T>G
|
|
|
NM_001305275.2:c.1824T>G
|
NP_001292204.1:p.Ala608=
|
|
NM_198576.4:c.1824T>G
MANE Select
|
NP_940978.2:p.Ala608=
|
|
NM_001364727.2:c.1509T>G
|
NP_001351656.1:p.Ala503=
|
|