ENST00000322213.9:c.3606A>G
MANE Select
|
ENSP00000323421.3:p.Gly1202=
|
|
ENST00000674590.1:c.2838A>G
|
ENSP00000502626.1:p.Gly946=
|
|
ENST00000675504.1:c.3540A>G
|
ENSP00000502524.1:p.Gly1180=
|
|
ENST00000322213.8:c.3606A>G
|
ENSP00000323421.3:p.Gly1202=
|
|
ENST00000375340.10:c.3540A>G
|
ENSP00000364489.7:p.Gly1180=
|
|
ENST00000470241.2:c.826A>G
|
|
|
NM_001281463.1:c.3540A>G , LRG_773t1:c.3540A>G
|
NP_001268392.1:p.Gly1180=
|
|
NM_006306.3:c.3606A>G , LRG_773t2:c.3606A>G
|
NP_006297.2:p.Gly1202=
|
|
NM_006306.4:c.3606A>G
MANE Select
|
NP_006297.2:p.Gly1202=
|
|