ENST00000394867.9:n.1590G>C
|
|
|
ENST00000688002.1:n.3302G>C
|
|
|
ENST00000688751.1:n.287G>C
|
|
|
ENST00000689792.1:n.1055G>C
|
|
|
ENST00000262948.10:c.1151G>C
MANE Select
|
ENSP00000262948.4:p.Cys384Ser
|
|
ENST00000262948.9:c.1151G>C
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ENSP00000262948.3:p.Cys384Ser
|
|
ENST00000394867.8:c.860G>C
|
ENSP00000378336.1:p.Cys287Ser
|
|
ENST00000597263.5:n.336G>C
|
|
|
ENST00000599021.1:c.261G>C
|
|
|
ENST00000600584.5:n.2600G>C
|
|
|
ENST00000601786.5:n.1452G>C
|
|
|
NM_030662.3:c.1151G>C , LRG_750t1:c.1151G>C
|
NP_109587.1:p.Cys384Ser
|
|
XM_006722799.2:c.872G>C
|
XP_006722862.1:p.Cys291Ser
|
|
XM_011528133.1:c.581G>C
|
XP_011526435.1:p.Cys194Ser
|
|
NM_030662.4:c.1151G>C
MANE Select
|
NP_109587.1:p.Cys384Ser
|
|