ENST00000356839.10:c.1936G>T
MANE Select
|
ENSP00000349297.5:p.Gly646Cys
|
|
ENST00000322910.9:c.*1891G>T
|
ENSP00000325395.5:n.*1891G>T
|
|
ENST00000350303.9:c.1870G>T
|
ENSP00000344152.5:p.Gly624Cys
|
|
ENST00000356839.9:c.1936G>T
|
ENSP00000349297.5:p.Gly646Cys
|
|
ENST00000542255.6:c.815G>T
|
|
|
ENST00000543245.6:c.2005G>T
|
ENSP00000438689.2:p.Gly669Cys
|
|
ENST00000578033.1:n.361G>T
|
|
|
ENST00000578319.5:n.517G>T
|
|
|
ENST00000578711.1:n.1561G>T
|
|
|
ENST00000578809.5:n.508G>T
|
|
|
ENST00000579425.5:n.1052G>T
|
|
|
ENST00000583848.5:c.302G>T
|
ENSP00000466487.1:n.302G>T
|
|
ENST00000583850.5:n.707G>T
|
|
|
ENST00000583858.5:c.867G>T
|
|
|
NM_000018.3:c.1936G>T
|
NP_000009.1:p.Gly646Cys
|
|
NM_001033859.2:c.1870G>T
|
NP_001029031.1:p.Gly624Cys
|
|
NM_001270447.1:c.2005G>T
|
NP_001257376.1:p.Gly669Cys
|
|
NM_001270448.1:c.1708G>T
|
NP_001257377.1:p.Gly570Cys
|
|
XM_006721516.2:c.1957G>T
|
XP_006721579.2:p.Gly653Cys
|
|
XM_011523829.1:c.1855G>T
|
XP_011522131.1:p.Gly619Cys
|
|
XM_011523830.1:c.1834G>T
|
XP_011522132.1:p.Gly612Cys
|
|
XR_934021.1:n.2039G>T
|
|
|
XR_934022.1:n.1945G>T
|
|
|
XR_934023.1:n.1966G>T
|
|
|
XM_006721516.3:c.1957G>T
|
XP_006721579.2:p.Gly653Cys
|
|
XM_011523829.2:c.1855G>T
|
XP_011522131.1:p.Gly619Cys
|
|
XM_011523830.2:c.1834G>T
|
XP_011522132.1:p.Gly612Cys
|
|
XM_024450741.1:c.1924G>T
|
XP_024306509.1:p.Gly642Cys
|
|
XR_934021.2:n.1991G>T
|
|
|
XR_934022.2:n.1897G>T
|
|
|
XR_934023.2:n.1918G>T
|
|
|
NM_000018.4:c.1936G>T
MANE Select
|
NP_000009.1:p.Gly646Cys
|
|
NM_001033859.3:c.1870G>T
|
NP_001029031.1:p.Gly624Cys
|
|
NM_001270447.2:c.2005G>T
|
NP_001257376.1:p.Gly669Cys
|
|
NM_001270448.2:c.1708G>T
|
NP_001257377.1:p.Gly570Cys
|
|