ENST00000348974.5:c.1563T>A
|
ENSP00000330021.7:p.Gly521=
|
|
ENST00000394236.9:c.1563T>A
MANE Select
|
ENSP00000377783.3:p.Gly521=
|
|
ENST00000407433.6:c.1518T>A
|
ENSP00000385794.2:p.Gly506=
|
|
ENST00000647936.1:c.1563T>A
|
ENSP00000496822.1:p.Gly521=
|
|
ENST00000648381.1:n.1731T>A
|
|
|
ENST00000648853.1:c.1521T>A
|
ENSP00000497262.1:p.Gly507=
|
|
ENST00000649103.1:c.1662T>A
|
ENSP00000497962.1:n.1662T>A
|
|
ENST00000649585.1:c.506T>A
|
ENSP00000498163.1:n.506T>A
|
|
ENST00000650591.1:c.1659T>A
|
ENSP00000497376.1:p.Gly553=
|
|
ENST00000394236.7:c.1563T>A
|
ENSP00000377783.3:p.Gly521=
|
|
ENST00000407433.5:c.1170T>A
|
ENSP00000385794.1:p.Gly390=
|
|
NM_000313.3:c.1563T>A , LRG_572t1:c.1563T>A
|
NP_000304.2:p.Gly521=
|
|
NM_001314077.1:c.1659T>A , LRG_572t2:c.1659T>A
|
NP_001301006.1:p.Gly553=
|
|
NM_000313.4:c.1563T>A
MANE Select
|
NP_000304.2:p.Gly521=
|
|
NM_001314077.2:c.1659T>A
|
NP_001301006.1:p.Gly553=
|
|