ENST00000379644.9:c.1835A>G
MANE Select
|
ENSP00000368965.4:p.Asn612Ser
|
|
ENST00000379644.8:c.1835A>G
|
ENSP00000368965.4:p.Asn612Ser
|
|
ENST00000519705.1:n.1151A>G
|
|
|
ENST00000521576.1:c.986A>G
|
ENSP00000429029.1:p.Asn329Ser
|
|
NM_152419.2:c.1835A>G
|
NP_689632.2:p.Asn612Ser
|
|
XM_005273409.1:c.1946A>G
|
XP_005273466.1:p.Asn649Ser
|
|
XM_005273410.1:c.1922A>G
|
XP_005273467.1:p.Asn641Ser
|
|
XM_005273411.1:c.1754A>G
|
XP_005273468.1:p.Asn585Ser
|
|
NM_001363227.1:c.1922A>G
|
NP_001350156.1:p.Asn641Ser
|
|
NM_001363228.1:c.1643A>G
|
NP_001350157.1:p.Asn548Ser
|
|
NM_001363229.1:c.971A>G
|
NP_001350158.1:p.Asn324Ser
|
|
NM_152419.3:c.1835A>G
MANE Select
|
NP_689632.2:p.Asn612Ser
|
|
NM_001363227.2:c.1922A>G
|
NP_001350156.1:p.Asn641Ser
|
|
NM_001363228.2:c.1643A>G
|
NP_001350157.1:p.Asn548Ser
|
|
NM_001363229.2:c.971A>G
|
NP_001350158.1:p.Asn324Ser
|
|