ENST00000394867.9:n.1444C>G
|
|
|
ENST00000688002.1:n.3156C>G
|
|
|
ENST00000688751.1:n.141C>G
|
|
|
ENST00000689792.1:n.909C>G
|
|
|
ENST00000262948.10:c.1005C>G
MANE Select
|
ENSP00000262948.4:p.Asn335Lys
|
|
ENST00000262948.9:c.1005C>G
|
ENSP00000262948.3:p.Asn335Lys
|
|
ENST00000394867.8:c.714C>G
|
ENSP00000378336.1:p.Asn238Lys
|
|
ENST00000595715.1:n.820C>G
|
|
|
ENST00000597263.5:n.190C>G
|
|
|
ENST00000599021.1:c.115C>G
|
|
|
ENST00000600584.5:n.1565C>G
|
|
|
ENST00000601786.5:n.1306C>G
|
|
|
NM_030662.3:c.1005C>G , LRG_750t1:c.1005C>G
|
NP_109587.1:p.Asn335Lys
|
|
XM_006722799.2:c.726C>G
|
XP_006722862.1:p.Asn242Lys
|
|
XM_011528133.1:c.435C>G
|
XP_011526435.1:p.Asn145Lys
|
|
XM_017026989.1:c.1005C>G
|
XP_016882478.1:p.Asn335Lys
|
|
XM_017026990.1:c.726C>G
|
XP_016882479.1:p.Asn242Lys
|
|
NM_030662.4:c.1005C>G
MANE Select
|
NP_109587.1:p.Asn335Lys
|
|