ENST00000433473.8:c.862C>A
|
ENSP00000394863.4:p.His288Asn
|
|
ENST00000439754.6:c.793C>A
|
ENSP00000403207.2:p.His265Asn
|
|
ENST00000449045.7:c.556C>A
|
ENSP00000392293.2:p.His186Asn
|
|
ENST00000530076.6:c.208C>A
|
ENSP00000434007.1:p.His70Asn
|
|
ENST00000530704.6:c.*488C>A
|
ENSP00000431655.1:n.*488C>A
|
|
ENST00000641083.1:c.955C>A
|
|
|
ENST00000641236.1:n.1102C>A
|
|
|
ENST00000641319.1:c.*75C>A
|
ENSP00000493128.1:n.*75C>A
|
|
ENST00000641381.1:c.287C>A
|
|
|
ENST00000641471.1:c.952C>A
|
ENSP00000493146.1:p.His318Asn
|
|
ENST00000641691.1:c.*717C>A
|
ENSP00000492910.1:n.*717C>A
|
|
ENST00000641924.1:c.*294C>A
|
ENSP00000493063.1:n.*294C>A
|
|
ENST00000642050.2:c.865C>A
MANE Select
|
ENSP00000493153.1:p.His289Asn
|
|
ENST00000372775.2:n.262C>A
|
|
|
ENST00000433473.7:c.865C>A
|
ENSP00000394863.3:p.His289Asn
|
|
ENST00000439754.5:c.478C>A
|
ENSP00000403207.1:p.His160Asn
|
|
ENST00000449045.6:c.556C>A
|
ENSP00000392293.2:p.His186Asn
|
|
ENST00000529905.5:c.865C>A
|
ENSP00000432053.1:p.His289Asn
|
|
ENST00000530076.5:c.208C>A
|
ENSP00000434007.1:p.His70Asn
|
|
ENST00000530704.5:c.*488C>A
|
ENSP00000431655.1:n.*488C>A
|
|
NM_000310.3:c.865C>A , LRG_690t1:c.865C>A
|
NP_000301.1:p.His289Asn
|
|
NM_001142604.1:c.556C>A
|
NP_001136076.1:p.His186Asn
|
|
XM_005271008.1:c.793C>A
|
XP_005271065.1:p.His265Asn
|
|
NM_001363695.1:c.793C>A
|
NP_001350624.1:p.His265Asn
|
|
NM_000310.4:c.865C>A
MANE Select
|
NP_000301.1:p.His289Asn
|
|
NM_001142604.2:c.556C>A
|
NP_001136076.1:p.His186Asn
|
|
NM_001363695.2:c.793C>A
|
NP_001350624.1:p.His265Asn
|
|