|
ENST00000356839.10:c.1567G>C
MANE Select
|
ENSP00000349297.5:p.Gly523Arg
|
|
|
ENST00000322910.9:c.*1522G>C
|
ENSP00000325395.5:n.*1522G>C
|
|
|
ENST00000350303.9:c.1501G>C
|
ENSP00000344152.5:p.Gly501Arg
|
|
|
ENST00000356839.9:c.1567G>C
|
ENSP00000349297.5:p.Gly523Arg
|
|
|
ENST00000542255.6:c.425G>C
|
|
|
|
ENST00000543245.6:c.1636G>C
|
ENSP00000438689.2:p.Gly546Arg
|
|
|
ENST00000578319.5:n.62G>C
|
|
|
|
ENST00000578711.1:n.851G>C
|
|
|
|
ENST00000578809.5:n.139G>C
|
|
|
|
ENST00000579391.1:n.175G>C
|
|
|
|
ENST00000579425.5:n.683G>C
|
|
|
|
ENST00000579546.1:c.306G>C
|
|
|
|
ENST00000579894.5:n.354G>C
|
|
|
|
ENST00000582450.1:n.75G>C
|
|
|
|
ENST00000583074.5:n.188G>C
|
|
|
|
ENST00000583850.5:n.342G>C
|
|
|
|
ENST00000583858.5:c.498G>C
|
|
|
|
ENST00000585203.6:n.758G>C
|
|
|
|
NM_000018.3:c.1567G>C
|
NP_000009.1:p.Gly523Arg
|
|
|
NM_001033859.2:c.1501G>C
|
NP_001029031.1:p.Gly501Arg
|
|
|
NM_001270447.1:c.1636G>C
|
NP_001257376.1:p.Gly546Arg
|
|
|
NM_001270448.1:c.1339G>C
|
NP_001257377.1:p.Gly447Arg
|
|
|
XM_006721516.2:c.1567G>C
|
XP_006721579.2:p.Gly523Arg
|
|
|
XM_011523829.1:c.1469G>C
|
XP_011522131.1:p.Arg490Pro
|
|
|
XM_011523830.1:c.1469G>C
|
XP_011522132.1:p.Arg490Pro
|
|
|
XR_934021.1:n.1674G>C
|
|
|
|
XR_934022.1:n.1576G>C
|
|
|
|
XR_934023.1:n.1576G>C
|
|
|
|
XM_006721516.3:c.1567G>C
|
XP_006721579.2:p.Gly523Arg
|
|
|
XM_011523829.2:c.1469G>C
|
XP_011522131.1:p.Arg490Pro
|
|
|
XM_011523830.2:c.1469G>C
|
XP_011522132.1:p.Arg490Pro
|
|
|
XM_024450741.1:c.1469G>C
|
XP_024306509.1:p.Arg490Pro
|
|
|
XR_934021.2:n.1626G>C
|
|
|
|
XR_934022.2:n.1528G>C
|
|
|
|
XR_934023.2:n.1528G>C
|
|
|
|
NM_000018.4:c.1567G>C
MANE Select
|
NP_000009.1:p.Gly523Arg
|
|
|
NM_001033859.3:c.1501G>C
|
NP_001029031.1:p.Gly501Arg
|
|
|
NM_001270447.2:c.1636G>C
|
NP_001257376.1:p.Gly546Arg
|
|
|
NM_001270448.2:c.1339G>C
|
NP_001257377.1:p.Gly447Arg
|
|
