ENST00000346342.8:c.745C>A
MANE Select
|
ENSP00000329546.4:p.His249Asn
|
|
ENST00000346342.7:c.745C>A
|
ENSP00000329546.3:p.His249Asn
|
|
ENST00000375581.3:c.811C>A
|
ENSP00000364731.3:p.His271Asn
|
|
ENST00000541084.5:c.559C>A
|
ENSP00000442051.2:p.His187Asn
|
|
NM_000131.4:c.811C>A , LRG_554t1:c.811C>A
|
NP_000122.1:p.His271Asn
|
|
NM_001267554.1:c.559C>A
|
NP_001254483.1:p.His187Asn
|
|
NM_019616.3:c.745C>A , LRG_554t2:c.745C>A
|
NP_062562.1:p.His249Asn
|
|
NR_051961.1:n.832C>A
|
|
|
XM_006719963.2:c.604C>A
|
XP_006720026.1:p.His202Asn
|
|
XM_011537474.1:c.853C>A
|
XP_011535776.1:p.His285Asn
|
|
XM_011537475.1:c.667C>A
|
XP_011535777.1:p.His223Asn
|
|
XM_011537476.1:c.505C>A
|
XP_011535778.1:p.His169Asn
|
|
XM_011537477.1:c.814C>A
|
XP_011535779.1:p.His272Asn
|
|
XM_006719963.3:c.649C>A
|
XP_006720026.2:p.His217Asn
|
|
XM_011537474.2:c.898C>A
|
XP_011535776.2:p.His300Asn
|
|
XM_011537475.2:c.712C>A
|
XP_011535777.2:p.His238Asn
|
|
XM_011537476.2:c.505C>A
|
XP_011535778.1:p.His169Asn
|
|
NM_019616.4:c.745C>A
MANE Select
|
NP_062562.1:p.His249Asn
|
|
NR_051961.2:n.829C>A
|
|
|
NM_001267554.2:c.559C>A
|
NP_001254483.1:p.His187Asn
|
|