ENST00000264414.9:c.1367C=
MANE Select
|
ENSP00000264414.4:p.Ser456=
|
|
ENST00000264414.8:c.1367C=
|
ENSP00000264414.4:p.Ser456=
|
|
ENST00000344951.8:c.1169C=
|
ENSP00000343601.4:p.Ser390=
|
|
ENST00000409096.5:c.1295C=
|
ENSP00000387200.1:p.Ser432=
|
|
ENST00000409777.5:c.1295C=
|
ENSP00000386525.1:p.Ser432=
|
|
ENST00000481135.1:n.663C=
|
|
|
ENST00000617432.4:c.89C=
|
ENSP00000477851.1:p.Ser30=
|
|
NM_001257197.1:c.1169C=
|
NP_001244126.1:p.Ser390=
|
|
NM_001257198.1:c.1385C=
|
NP_001244127.1:p.Ser462=
|
|
NM_003590.4:c.1367C=
|
NP_003581.1:p.Ser456=
|
|
XM_006712800.2:c.1334C=
|
XP_006712863.2:p.Ser445=
|
|
XM_011511994.1:c.1220C=
|
XP_011510296.1:p.Ser407=
|
|
XM_011511995.1:c.1325C=
|
XP_011510297.1:p.Ser442=
|
|
XM_011511996.1:c.1175C=
|
XP_011510298.1:p.Ser392=
|
|
XM_011511997.1:c.1067C=
|
XP_011510299.1:p.Ser356=
|
|
XM_011511994.3:c.1220C=
|
XP_011510296.1:p.Ser407=
|
|
XM_011511996.2:c.1175C=
|
XP_011510298.1:p.Ser392=
|
|
NM_003590.5:c.1367C=
MANE Select
|
NP_003581.1:p.Ser456=
|
|
NM_001257198.2:c.1385C=
|
NP_001244127.1:p.Ser462=
|
|
NM_001257197.2:c.1169C=
|
NP_001244126.1:p.Ser390=
|
|