ENST00000389048.8:c.3556A>C
MANE Select
|
ENSP00000373700.3:p.Ser1186Arg
|
|
ENST00000431873.6:c.783A>C
|
|
|
ENST00000638605.1:n.433A>C
|
|
|
ENST00000642122.1:c.352A>C
|
ENSP00000493203.1:p.Ser118Arg
|
|
ENST00000389048.7:c.3556A>C
|
ENSP00000373700.3:p.Ser1186Arg
|
|
ENST00000431873.5:c.436A>C
|
ENSP00000414027.2:p.Ser146Arg
|
|
ENST00000618119.4:c.2425A>C
|
ENSP00000482733.1:p.Ser809Arg
|
|
NM_004304.4:c.3556A>C
|
NP_004295.2:p.Ser1186Arg
|
|
NM_001353765.1:c.352A>C
|
NP_001340694.1:p.Ser118Arg
|
|
XM_024452778.1:c.709A>C
|
XP_024308546.1:p.Ser237Arg
|
|
XM_024452779.1:c.352A>C
|
XP_024308547.1:p.Ser118Arg
|
|
NM_004304.5:c.3556A>C
MANE Select
|
NP_004295.2:p.Ser1186Arg
|
|
NM_001353765.2:c.352A>C
|
NP_001340694.1:p.Ser118Arg
|
|