NM_001159.4:c.3404A>G
MANE Select
|
NP_001150.3:p.Asn1135Ser
|
ENST00000374700.7:c.3404A>G
MANE Select
|
ENSP00000363832.2:p.Asn1135Ser
|
NM_001159.3:c.3404A>G
|
NP_001150.3:p.Asn1135Ser
|
ENST00000260930.10:c.62A>G
|
ENSP00000260930.6:p.Asn21Ser
|
ENST00000374700.6:c.3404A>G
|
ENSP00000363832.2:p.Asn1135Ser
|
ENST00000465297.5:n.2336A>G
|
|
ENST00000485106.5:n.2143A>G
|
|
XM_011511062.1:c.3404A>G
|
XP_011509364.1:p.Asn1135Ser
|
XM_017003946.1:c.3404A>G
|
XP_016859435.1:p.Asn1135Ser
|
XM_017003947.2:c.3404A>G
|
XP_016859436.1:p.Asn1135Ser
|
XR_922913.1:n.3561A>G
|
|