ENST00000389048.8:c.3524A>G
MANE Select
|
ENSP00000373700.3:p.Asn1175Ser
|
|
ENST00000431873.6:c.751A>G
|
|
|
ENST00000638605.1:n.401A>G
|
|
|
ENST00000642122.1:c.320A>G
|
ENSP00000493203.1:p.Asn107Ser
|
|
ENST00000389048.7:c.3524A>G
|
ENSP00000373700.3:p.Asn1175Ser
|
|
ENST00000431873.5:c.404A>G
|
ENSP00000414027.2:p.Asn135Ser
|
|
ENST00000618119.4:c.2393A>G
|
ENSP00000482733.1:p.Asn798Ser
|
|
NM_004304.4:c.3524A>G
|
NP_004295.2:p.Asn1175Ser
|
|
NM_001353765.1:c.320A>G
|
NP_001340694.1:p.Asn107Ser
|
|
XM_024452778.1:c.677A>G
|
XP_024308546.1:p.Asn226Ser
|
|
XM_024452779.1:c.320A>G
|
XP_024308547.1:p.Asn107Ser
|
|
NM_004304.5:c.3524A>G
MANE Select
|
NP_004295.2:p.Asn1175Ser
|
|
NM_001353765.2:c.320A>G
|
NP_001340694.1:p.Asn107Ser
|
|