ENST00000389048.8:c.3532A>C
MANE Select
|
ENSP00000373700.3:p.Asn1178His
|
|
ENST00000431873.6:c.759A>C
|
|
|
ENST00000638605.1:n.409A>C
|
|
|
ENST00000642122.1:c.328A>C
|
ENSP00000493203.1:p.Asn110His
|
|
ENST00000389048.7:c.3532A>C
|
ENSP00000373700.3:p.Asn1178His
|
|
ENST00000431873.5:c.412A>C
|
ENSP00000414027.2:p.Asn138His
|
|
ENST00000618119.4:c.2401A>C
|
ENSP00000482733.1:p.Asn801His
|
|
NM_004304.4:c.3532A>C
|
NP_004295.2:p.Asn1178His
|
|
NM_001353765.1:c.328A>C
|
NP_001340694.1:p.Asn110His
|
|
XM_024452778.1:c.685A>C
|
XP_024308546.1:p.Asn229His
|
|
XM_024452779.1:c.328A>C
|
XP_024308547.1:p.Asn110His
|
|
NM_004304.5:c.3532A>C
MANE Select
|
NP_004295.2:p.Asn1178His
|
|
NM_001353765.2:c.328A>C
|
NP_001340694.1:p.Asn110His
|
|