ENST00000346342.8:c.364C>A
MANE Select
|
ENSP00000329546.4:p.His122Asn
|
|
ENST00000346342.7:c.364C>A
|
ENSP00000329546.3:p.His122Asn
|
|
ENST00000375581.3:c.430C>A
|
ENSP00000364731.3:p.His144Asn
|
|
ENST00000444337.1:c.*172C>A
|
ENSP00000387669.1:n.*172C>A
|
|
ENST00000473085.1:n.311C>A
|
|
|
ENST00000479674.1:n.697C>A
|
|
|
ENST00000541084.5:c.178C>A
|
ENSP00000442051.2:p.His60Asn
|
|
NM_000131.4:c.430C>A , LRG_554t1:c.430C>A
|
NP_000122.1:p.His144Asn
|
|
NM_001267554.1:c.178C>A
|
NP_001254483.1:p.His60Asn
|
|
NM_019616.3:c.364C>A , LRG_554t2:c.364C>A
|
NP_062562.1:p.His122Asn
|
|
NR_051961.1:n.451C>A
|
|
|
XM_006719963.2:c.364C>A
|
XP_006720026.1:p.Leu122Ile
|
|
XM_011537474.1:c.364C>A
|
XP_011535776.1:p.Gln122Lys
|
|
XM_011537475.1:c.178C>A
|
XP_011535777.1:p.Gln60Lys
|
|
XM_011537477.1:c.325C>A
|
XP_011535779.1:p.Gln109Lys
|
|
XM_006719963.3:c.409C>A
|
XP_006720026.2:p.Leu137Ile
|
|
XM_011537474.2:c.409C>A
|
XP_011535776.2:p.Gln137Lys
|
|
XM_011537475.2:c.223C>A
|
XP_011535777.2:p.Gln75Lys
|
|
NM_019616.4:c.364C>A
MANE Select
|
NP_062562.1:p.His122Asn
|
|
NR_051961.2:n.448C>A
|
|
|
NM_001267554.2:c.178C>A
|
NP_001254483.1:p.His60Asn
|
|