|
ENST00000375687.10:c.3886A>C
MANE Select
|
ENSP00000364839.4:p.Asn1296His
|
|
|
ENST00000646985.1:c.3703A>C
|
ENSP00000495053.1:p.Asn1235His
|
|
|
ENST00000647223.1:n.6239A>C
|
|
|
|
ENST00000651418.1:c.1870-1832A>C
|
ENSP00000499150.1:n.1870-1832A>C
|
|
|
ENST00000306058.9:c.3871A>C
|
ENSP00000305119.5:p.Asn1291His
|
|
|
ENST00000375687.8:c.3886A>C
|
ENSP00000364839.4:p.Asn1296His
|
|
|
ENST00000613218.4:c.3886A>C
|
ENSP00000480487.1:p.Asn1296His
|
|
|
ENST00000620121.4:c.3886A>C
|
ENSP00000481978.1:p.Asn1296His
|
|
|
NM_015338.5:c.3886A>C , LRG_630t1:c.3886A>C
|
NP_056153.2:p.Asn1296His
|
|
|
XM_006723727.2:c.3883A>C
|
XP_006723790.1:p.Asn1295His
|
|
|
XM_006723728.2:c.3856A>C
|
XP_006723791.1:p.Asn1286His
|
|
|
XM_006723730.2:c.3802A>C
|
XP_006723793.1:p.Asn1268His
|
|
|
XM_006723732.2:c.3703A>C
|
XP_006723795.1:p.Asn1235His
|
|
|
XM_006723733.1:c.3202A>C
|
XP_006723796.1:p.Asn1068His
|
|
|
XM_011528647.1:c.4150A>C
|
XP_011526949.1:p.Asn1384His
|
|
|
XM_011528648.1:c.4147A>C
|
XP_011526950.1:p.Asn1383His
|
|
|
XM_011528649.1:c.4066A>C
|
XP_011526951.1:p.Asn1356His
|
|
|
XM_011528650.1:c.3997A>C
|
XP_011526952.1:p.Asn1333His
|
|
|
XM_011528651.1:c.3865A>C
|
XP_011526953.1:p.Asn1289His
|
|
|
XM_011528652.1:c.3802A>C
|
XP_011526954.1:p.Asn1268His
|
|
|
NM_001363734.1:c.3703A>C
|
NP_001350663.1:p.Asn1235His
|
|
|
XM_006723727.3:c.3883A>C
|
XP_006723790.1:p.Asn1295His
|
|
|
XM_006723728.3:c.3856A>C
|
XP_006723791.1:p.Asn1286His
|
|
|
XM_006723730.4:c.3802A>C
|
XP_006723793.1:p.Asn1268His
|
|
|
XM_011528648.3:c.4147A>C
|
XP_011526950.1:p.Asn1383His
|
|
|
XM_011528652.2:c.3802A>C
|
XP_011526954.1:p.Asn1268His
|
|
|
XM_017027704.1:c.3802A>C
|
XP_016883193.1:p.Asn1268His
|
|
|
XM_017027705.1:c.3802A>C
|
XP_016883194.1:p.Asn1268His
|
|
|
XM_017027706.1:c.3733A>C
|
XP_016883195.1:p.Asn1245His
|
|
|
NM_015338.6:c.3886A>C
MANE Select
|
NP_056153.2:p.Asn1296His
|
|
