ENST00000356839.10:c.1412T>C
MANE Select
|
ENSP00000349297.5:p.Phe471Ser
|
|
ENST00000322910.9:c.*1367T>C
|
ENSP00000325395.5:n.*1367T>C
|
|
ENST00000350303.9:c.1346T>C
|
ENSP00000344152.5:p.Phe449Ser
|
|
ENST00000356839.9:c.1412T>C
|
ENSP00000349297.5:p.Phe471Ser
|
|
ENST00000542255.6:c.270T>C
|
|
|
ENST00000543245.6:c.1481T>C
|
ENSP00000438689.2:p.Phe494Ser
|
|
ENST00000578711.1:n.543T>C
|
|
|
ENST00000579425.5:n.528T>C
|
|
|
ENST00000579546.1:c.249T>C
|
|
|
ENST00000579894.5:n.123T>C
|
|
|
ENST00000583074.5:n.131T>C
|
|
|
ENST00000583850.5:n.187T>C
|
|
|
ENST00000583858.5:c.441T>C
|
|
|
ENST00000585203.6:n.603T>C
|
|
|
NM_000018.3:c.1412T>C
|
NP_000009.1:p.Phe471Ser
|
|
NM_001033859.2:c.1346T>C
|
NP_001029031.1:p.Phe449Ser
|
|
NM_001270447.1:c.1481T>C
|
NP_001257376.1:p.Phe494Ser
|
|
NM_001270448.1:c.1184T>C
|
NP_001257377.1:p.Phe395Ser
|
|
XM_006721516.2:c.1412T>C
|
XP_006721579.2:p.Phe471Ser
|
|
XM_011523829.1:c.1412T>C
|
XP_011522131.1:p.Phe471Ser
|
|
XM_011523830.1:c.1412T>C
|
XP_011522132.1:p.Phe471Ser
|
|
XR_934021.1:n.1519T>C
|
|
|
XR_934022.1:n.1519T>C
|
|
|
XR_934023.1:n.1519T>C
|
|
|
XM_006721516.3:c.1412T>C
|
XP_006721579.2:p.Phe471Ser
|
|
XM_011523829.2:c.1412T>C
|
XP_011522131.1:p.Phe471Ser
|
|
XM_011523830.2:c.1412T>C
|
XP_011522132.1:p.Phe471Ser
|
|
XM_024450741.1:c.1412T>C
|
XP_024306509.1:p.Phe471Ser
|
|
XR_934021.2:n.1471T>C
|
|
|
XR_934022.2:n.1471T>C
|
|
|
XR_934023.2:n.1471T>C
|
|
|
NM_000018.4:c.1412T>C
MANE Select
|
NP_000009.1:p.Phe471Ser
|
|
NM_001033859.3:c.1346T>C
|
NP_001029031.1:p.Phe449Ser
|
|
NM_001270447.2:c.1481T>C
|
NP_001257376.1:p.Phe494Ser
|
|
NM_001270448.2:c.1184T>C
|
NP_001257377.1:p.Phe395Ser
|
|