ENST00000356978.9:c.291C>A
MANE Select
|
ENSP00000349467.4:p.Gly97=
|
|
ENST00000447653.8:c.183C>A
|
ENSP00000403491.4:p.Gly61=
|
|
ENST00000659177.1:c.183C>A
|
ENSP00000499421.1:p.Gly61=
|
|
ENST00000663135.1:c.183C>A
|
ENSP00000499498.1:p.Gly61=
|
|
ENST00000356978.8:c.291C>A
|
ENSP00000349467.4:p.Gly97=
|
|
ENST00000447653.7:c.294C>A
|
ENSP00000403491.3:p.Gly98=
|
|
ENST00000544280.6:c.183C>A
|
ENSP00000442853.2:p.Gly61=
|
|
ENST00000553422.1:c.178-15C>A
|
ENSP00000450425.1:n.178-15C>A
|
|
ENST00000553542.5:c.183C>A
|
ENSP00000450829.1:p.Gly61=
|
|
ENST00000553630.1:c.184C>A
|
ENSP00000451646.1:p.Gln62Lys
|
|
ENST00000553964.5:n.2421C>A
|
|
|
ENST00000554296.1:n.343C>A
|
|
|
ENST00000556721.1:n.217C>A
|
|
|
ENST00000557020.5:c.183C>A
|
ENSP00000451062.1:p.Gly61=
|
|
ENST00000626705.2:c.166-73C>A
|
ENSP00000486402.1:n.166-73C>A
|
|
NM_006888.4:c.291C>A
|
NP_008819.1:p.Gly97=
|
|
XM_006720258.2:c.294C>A
|
XP_006720321.1:p.Gly98=
|
|
NM_001363669.1:c.183C>A
|
NP_001350598.1:p.Gly61=
|
|
NM_001363670.1:c.294C>A
|
NP_001350599.1:p.Gly98=
|
|
NM_006888.5:c.291C>A
|
NP_008819.1:p.Gly97=
|
|
NM_006888.6:c.291C>A
MANE Select
|
NP_008819.1:p.Gly97=
|
|
NM_001363669.2:c.183C>A
|
NP_001350598.1:p.Gly61=
|
|
NM_001363670.2:c.294C>A
|
NP_001350599.1:p.Gly98=
|
|