ENST00000374552.9:c.937A>C
MANE Select
|
ENSP00000363680.4:p.Asn313His
|
|
ENST00000374552.8:c.937A>C
|
ENSP00000363680.4:p.Asn313His
|
|
ENST00000374553.6:c.931A>C
|
ENSP00000363681.2:p.Asn311His
|
|
ENST00000524573.5:c.922A>C
|
ENSP00000432585.1:p.Asn308His
|
|
ENST00000616899.1:c.541A>C
|
ENSP00000481963.1:p.Asn181His
|
|
NM_001005609.1:c.931A>C
|
NP_001005609.1:p.Asn311His
|
|
NM_001005612.2:c.922A>C
|
NP_001005612.2:p.Asn308His
|
|
NM_001399.4:c.937A>C
|
NP_001390.1:p.Asn313His
|
|
XM_006724630.2:c.928A>C
|
XP_006724693.1:p.Asn310His
|
|
XM_017029336.1:c.895A>C
|
XP_016884825.1:p.Asn299His
|
|
NM_001399.5:c.937A>C
MANE Select
|
NP_001390.1:p.Asn313His
|
|
NM_001005609.2:c.931A>C
|
NP_001005609.1:p.Asn311His
|
|
NM_001005612.3:c.922A>C
|
NP_001005612.2:p.Asn308His
|
|