ENST00000267845.8:c.1779T>C
MANE Select
|
ENSP00000267845.3:p.Ser593=
|
|
ENST00000267845.7:c.1779T>C
|
ENSP00000267845.3:p.Ser593=
|
|
ENST00000543581.5:c.1680T>C
|
ENSP00000440252.1:p.Ser560=
|
|
ENST00000559816.1:n.1523T>C
|
|
|
NM_001306146.1:c.1680T>C
|
NP_001293075.1:p.Ser560=
|
|
NM_002112.3:c.1779T>C
|
NP_002103.2:p.Ser593=
|
|
XM_011521479.1:c.1542T>C
|
XP_011519781.1:p.Ser514=
|
|
XM_011521480.1:c.1347T>C
|
XP_011519782.1:p.Ser449=
|
|
XM_017022094.1:c.1884T>C
|
XP_016877583.1:p.Ser628=
|
|
XM_017022095.1:c.1785T>C
|
XP_016877584.1:p.Ser595=
|
|
XM_017022096.1:c.1656T>C
|
XP_016877585.1:p.Ser552=
|
|
XM_017022097.1:c.1647T>C
|
XP_016877586.1:p.Ser549=
|
|
XM_017022098.1:c.1452T>C
|
XP_016877587.1:p.Ser484=
|
|
NM_002112.4:c.1779T>C
MANE Select
|
NP_002103.2:p.Ser593=
|
|
NM_001306146.2:c.1680T>C
|
NP_001293075.1:p.Ser560=
|
|