ENST00000330540.7:c.989A>G
MANE Select
|
ENSP00000332049.2:p.Ter330=
|
|
ENST00000264468.9:c.827A>G
|
ENSP00000264468.6:p.Ter276=
|
|
ENST00000330540.6:c.989A>G
|
ENSP00000332049.2:p.Ter330=
|
|
ENST00000393627.6:c.971A>G
|
ENSP00000377248.2:p.Ter324=
|
|
ENST00000469710.5:c.743A>G
|
ENSP00000418988.1:p.Ter248=
|
|
ENST00000478741.1:c.831A>G
|
|
|
ENST00000493101.5:c.653A>G
|
ENSP00000420230.1:p.Ter218=
|
|
NM_001206924.1:c.653A>G
|
NP_001193853.1:p.Ter218=
|
|
NM_001206925.1:c.743A>G
|
NP_001193854.1:p.Ter248=
|
|
NM_006889.4:c.971A>G
|
NP_008820.3:p.Ter324=
|
|
NM_175862.4:c.989A>G
|
NP_787058.4:p.Ter330=
|
|
NM_176892.1:c.827A>G
|
NP_795711.1:p.Ter276=
|
|
NM_175862.5:c.989A>G
MANE Select
|
NP_787058.5:p.Ter330=
|
|
NM_001206924.2:c.653A>G
|
NP_001193853.2:p.Ter218=
|
|
NM_001206925.2:c.743A>G
|
NP_001193854.2:p.Ter248=
|
|
NM_006889.5:c.971A>G
|
NP_008820.4:p.Ter324=
|
|
NM_176892.2:c.827A>G
|
NP_795711.2:p.Ter276=
|
|