ENST00000356839.10:c.1895G>C
MANE Select
|
ENSP00000349297.5:p.Arg632Pro
|
|
ENST00000322910.9:c.*1850G>C
|
ENSP00000325395.5:n.*1850G>C
|
|
ENST00000350303.9:c.1829G>C
|
ENSP00000344152.5:p.Arg610Pro
|
|
ENST00000356839.9:c.1895G>C
|
ENSP00000349297.5:p.Arg632Pro
|
|
ENST00000542255.6:c.774G>C
|
|
|
ENST00000543245.6:c.1964G>C
|
ENSP00000438689.2:p.Arg655Pro
|
|
ENST00000578033.1:n.320G>C
|
|
|
ENST00000578319.5:n.476G>C
|
|
|
ENST00000578711.1:n.1520G>C
|
|
|
ENST00000578809.5:n.467G>C
|
|
|
ENST00000579425.5:n.1011G>C
|
|
|
ENST00000583848.5:c.261G>C
|
ENSP00000466487.1:n.261G>C
|
|
ENST00000583850.5:n.666G>C
|
|
|
ENST00000583858.5:c.826G>C
|
|
|
NM_000018.3:c.1895G>C
|
NP_000009.1:p.Arg632Pro
|
|
NM_001033859.2:c.1829G>C
|
NP_001029031.1:p.Arg610Pro
|
|
NM_001270447.1:c.1964G>C
|
NP_001257376.1:p.Arg655Pro
|
|
NM_001270448.1:c.1667G>C
|
NP_001257377.1:p.Arg556Pro
|
|
XM_006721516.2:c.1916G>C
|
XP_006721579.2:p.Arg639Pro
|
|
XM_011523829.1:c.1814G>C
|
XP_011522131.1:p.Arg605Pro
|
|
XM_011523830.1:c.1793G>C
|
XP_011522132.1:p.Arg598Pro
|
|
XR_934021.1:n.1998G>C
|
|
|
XR_934022.1:n.1904G>C
|
|
|
XR_934023.1:n.1925G>C
|
|
|
XM_006721516.3:c.1916G>C
|
XP_006721579.2:p.Arg639Pro
|
|
XM_011523829.2:c.1814G>C
|
XP_011522131.1:p.Arg605Pro
|
|
XM_011523830.2:c.1793G>C
|
XP_011522132.1:p.Arg598Pro
|
|
XM_024450741.1:c.1883G>C
|
XP_024306509.1:p.Arg628Pro
|
|
XR_934021.2:n.1950G>C
|
|
|
XR_934022.2:n.1856G>C
|
|
|
XR_934023.2:n.1877G>C
|
|
|
NM_000018.4:c.1895G>C
MANE Select
|
NP_000009.1:p.Arg632Pro
|
|
NM_001033859.3:c.1829G>C
|
NP_001029031.1:p.Arg610Pro
|
|
NM_001270447.2:c.1964G>C
|
NP_001257376.1:p.Arg655Pro
|
|
NM_001270448.2:c.1667G>C
|
NP_001257377.1:p.Arg556Pro
|
|