ENST00000255078.8:c.2016C>A
MANE Select
|
ENSP00000255078.4:p.Ser672=
|
|
ENST00000674675.1:c.260C>A
|
|
|
ENST00000674878.1:c.260C>A
|
|
|
ENST00000674955.1:c.*733C>A
|
ENSP00000502463.1:n.*733C>A
|
|
ENST00000675118.1:c.1504C>A
|
|
|
ENST00000675389.1:n.291C>A
|
|
|
ENST00000675615.1:c.2016C>A
|
ENSP00000502413.1:p.Ser672=
|
|
ENST00000675648.1:n.1391C>A
|
|
|
ENST00000675916.1:c.260C>A
|
|
|
ENST00000676173.1:n.2761C>A
|
|
|
ENST00000676182.1:c.447C>A
|
|
|
ENST00000676228.1:c.*1339C>A
|
ENSP00000502375.1:n.*1339C>A
|
|
ENST00000255078.7:c.2016C>A
|
ENSP00000255078.3:p.Ser672=
|
|
ENST00000539064.5:n.1775C>A
|
|
|
ENST00000543739.5:n.1009C>A
|
|
|
NM_002180.2:c.2016C>A , LRG_250t1:c.2016C>A
|
NP_002171.2:p.Ser672=
|
|
XM_005273974.2:c.1005C>A
|
XP_005274031.1:p.Ser335=
|
|
XM_005273975.2:c.888C>A
|
XP_005274032.1:p.Ser296=
|
|
XM_011544994.1:c.783C>A
|
XP_011543296.1:p.Ser261=
|
|
XR_949903.1:n.2118C>A
|
|
|
XM_005273975.3:c.888C>A
|
XP_005274032.1:p.Ser296=
|
|
XM_017017669.2:c.1005C>A
|
XP_016873158.1:p.Ser335=
|
|
XM_017017670.2:c.1005C>A
|
XP_016873159.1:p.Ser335=
|
|
XR_949903.3:n.2114C>A
|
|
|
NM_002180.3:c.2016C>A
MANE Select
|
NP_002171.2:p.Ser672=
|
|