ENST00000696809.1:c.*1577G=
|
ENSP00000512887.1:n.*1577G=
|
|
ENST00000699276.1:c.*631G=
|
ENSP00000514257.1:n.*631G=
|
|
ENST00000323584.10:c.3003G=
MANE Select
|
ENSP00000313504.5:p.Glu1001=
|
|
ENST00000299167.12:c.3003G=
|
ENSP00000299167.8:p.Glu1001=
|
|
ENST00000323584.9:c.3003G=
|
ENSP00000313504.5:p.Glu1001=
|
|
ENST00000564711.2:c.17G=
|
|
|
ENST00000566044.5:c.2982G=
|
ENSP00000456729.1:p.Glu994=
|
|
ENST00000566319.2:n.1819G=
|
|
|
NM_000293.2:c.3003G=
|
NP_000284.1:p.Glu1001=
|
|
NM_001031835.2:c.2982G=
|
NP_001027005.1:p.Glu994=
|
|
XM_005255983.3:c.3003G=
|
XP_005256040.1:p.Glu1001=
|
|
XM_005255984.3:c.2982G=
|
XP_005256041.1:p.Glu994=
|
|
XM_011523107.1:c.1581G=
|
XP_011521409.1:p.Glu527=
|
|
NM_001363837.1:c.3003G=
|
NP_001350766.1:p.Glu1001=
|
|
XM_005255983.4:c.3003G=
|
XP_005256040.1:p.Glu1001=
|
|
XM_005255984.4:c.2982G=
|
XP_005256041.1:p.Glu994=
|
|
XM_017023282.1:c.1890G=
|
XP_016878771.1:p.Glu630=
|
|
XM_017023283.1:c.1581G=
|
XP_016878772.1:p.Glu527=
|
|
XM_017023284.1:c.1581G=
|
XP_016878773.1:p.Glu527=
|
|
XR_001751913.1:n.2927G=
|
|
|
NM_000293.3:c.3003G=
MANE Select
|
NP_000284.1:p.Glu1001=
|
|
NM_001031835.3:c.2982G=
|
NP_001027005.1:p.Glu994=
|
|