ENST00000682275.1:c.1893T>G
|
ENSP00000507852.1:p.Ser631=
|
|
ENST00000683395.1:c.1834T>G
|
|
|
ENST00000684087.1:c.1857T>G
|
ENSP00000506978.1:p.Ser619=
|
|
ENST00000506362.2:c.1608T>G
|
ENSP00000424103.2:p.Ser536=
|
|
ENST00000673642.1:c.1516T>G
|
ENSP00000501242.1:n.1516T>G
|
|
ENST00000673991.1:c.1893T>G
|
ENSP00000501033.1:p.Ser631=
|
|
ENST00000226760.5:c.1857T>G
MANE Select
|
ENSP00000226760.1:p.Ser619=
|
|
ENST00000503569.5:c.1857T>G
|
ENSP00000423337.1:p.Ser619=
|
|
ENST00000507765.1:n.2042T>G
|
|
|
NM_001145853.1:c.1857T>G
|
NP_001139325.1:p.Ser619=
|
|
NM_006005.3:c.1857T>G
MANE Select
|
NP_005996.2:p.Ser619=
|
|
XM_017008586.1:c.1866T>G
|
XP_016864075.1:p.Ser622=
|
|