ENST00000394867.9:n.1532A>C
|
|
|
ENST00000688002.1:n.3244A>C
|
|
|
ENST00000688751.1:n.229A>C
|
|
|
ENST00000689792.1:n.997A>C
|
|
|
ENST00000262948.10:c.1093A>C
MANE Select
|
ENSP00000262948.4:p.Asn365His
|
|
ENST00000262948.9:c.1093A>C
|
ENSP00000262948.3:p.Asn365His
|
|
ENST00000394867.8:c.802A>C
|
ENSP00000378336.1:p.Asn268His
|
|
ENST00000597263.5:n.278A>C
|
|
|
ENST00000599021.1:c.203A>C
|
|
|
ENST00000600584.5:n.2542A>C
|
|
|
ENST00000601786.5:n.1394A>C
|
|
|
NM_030662.3:c.1093A>C , LRG_750t1:c.1093A>C
|
NP_109587.1:p.Asn365His
|
|
XM_006722799.2:c.814A>C
|
XP_006722862.1:p.Asn272His
|
|
XM_011528133.1:c.523A>C
|
XP_011526435.1:p.Asn175His
|
|
NM_030662.4:c.1093A>C
MANE Select
|
NP_109587.1:p.Asn365His
|
|