ENST00000336411.7:c.1352G=
|
ENSP00000337915.3:p.Ser451=
|
|
ENST00000651162.1:n.694G=
|
|
|
ENST00000651514.1:c.1259G=
MANE Select
|
ENSP00000498939.1:p.Ser420=
|
|
ENST00000651783.1:c.800G=
|
ENSP00000498924.1:p.Ser267=
|
|
ENST00000652018.1:c.1112G=
|
ENSP00000498733.1:p.Ser371=
|
|
ENST00000336411.6:c.1259G=
|
ENSP00000337915.2:p.Ser420=
|
|
ENST00000354593.6:c.809G=
|
ENSP00000346607.2:p.Ser270=
|
|
NM_001202855.2:c.1256G=
|
NP_001189784.1:p.Ser419=
|
|
NM_017460.5:c.1259G=
|
NP_059488.2:p.Ser420=
|
|
XM_011515841.1:c.1352G=
|
XP_011514143.1:p.Ser451=
|
|
XM_011515842.1:c.1349G=
|
XP_011514144.1:p.Ser450=
|
|
NM_017460.6:c.1259G=
MANE Select
|
NP_059488.2:p.Ser420=
|
|
NM_001202855.3:c.1256G=
|
NP_001189784.1:p.Ser419=
|
|