ENST00000394867.9:n.1149A>C
|
|
|
ENST00000687128.1:n.1149A>C
|
|
|
ENST00000688002.1:n.1004A>C
|
|
|
ENST00000689792.1:n.646-32A>C
|
|
|
ENST00000262948.10:c.710A>C
MANE Select
|
ENSP00000262948.4:p.Glu237Ala
|
|
ENST00000262948.9:c.710A>C
|
ENSP00000262948.3:p.Glu237Ala
|
|
ENST00000394867.8:c.419A>C
|
ENSP00000378336.1:p.Glu140Ala
|
|
ENST00000593364.5:n.657A>C
|
|
|
ENST00000595715.1:n.525A>C
|
|
|
ENST00000597263.5:n.169+1609A>C
|
|
|
ENST00000599021.1:c.29+1609A>C
|
|
|
ENST00000600584.5:n.1270A>C
|
|
|
ENST00000601786.5:n.1011A>C
|
|
|
ENST00000602167.5:n.430A>C
|
|
|
NM_030662.3:c.710A>C , LRG_750t1:c.710A>C
|
NP_109587.1:p.Glu237Ala
|
|
XM_006722799.2:c.705+1609A>C
|
XP_006722862.1:n.705+1609A>C
|
|
XM_011528133.1:c.140A>C
|
XP_011526435.1:p.Glu47Ala
|
|
XM_017026989.1:c.710A>C
|
XP_016882478.1:p.Glu237Ala
|
|
XM_017026990.1:c.705+1609A>C
|
XP_016882479.1:n.705+1609A>C
|
|
NM_030662.4:c.710A>C
MANE Select
|
NP_109587.1:p.Glu237Ala
|
|