ENST00000356839.10:c.1918G>C
MANE Select
|
ENSP00000349297.5:p.Ala640Pro
|
|
ENST00000322910.9:c.*1873G>C
|
ENSP00000325395.5:n.*1873G>C
|
|
ENST00000350303.9:c.1852G>C
|
ENSP00000344152.5:p.Ala618Pro
|
|
ENST00000356839.9:c.1918G>C
|
ENSP00000349297.5:p.Ala640Pro
|
|
ENST00000542255.6:c.797G>C
|
|
|
ENST00000543245.6:c.1987G>C
|
ENSP00000438689.2:p.Ala663Pro
|
|
ENST00000578033.1:n.343G>C
|
|
|
ENST00000578319.5:n.499G>C
|
|
|
ENST00000578711.1:n.1543G>C
|
|
|
ENST00000578809.5:n.490G>C
|
|
|
ENST00000579425.5:n.1034G>C
|
|
|
ENST00000583848.5:c.284G>C
|
ENSP00000466487.1:n.284G>C
|
|
ENST00000583850.5:n.689G>C
|
|
|
ENST00000583858.5:c.849G>C
|
|
|
NM_000018.3:c.1918G>C
|
NP_000009.1:p.Ala640Pro
|
|
NM_001033859.2:c.1852G>C
|
NP_001029031.1:p.Ala618Pro
|
|
NM_001270447.1:c.1987G>C
|
NP_001257376.1:p.Ala663Pro
|
|
NM_001270448.1:c.1690G>C
|
NP_001257377.1:p.Ala564Pro
|
|
XM_006721516.2:c.1939G>C
|
XP_006721579.2:p.Ala647Pro
|
|
XM_011523829.1:c.1837G>C
|
XP_011522131.1:p.Ala613Pro
|
|
XM_011523830.1:c.1816G>C
|
XP_011522132.1:p.Ala606Pro
|
|
XR_934021.1:n.2021G>C
|
|
|
XR_934022.1:n.1927G>C
|
|
|
XR_934023.1:n.1948G>C
|
|
|
XM_006721516.3:c.1939G>C
|
XP_006721579.2:p.Ala647Pro
|
|
XM_011523829.2:c.1837G>C
|
XP_011522131.1:p.Ala613Pro
|
|
XM_011523830.2:c.1816G>C
|
XP_011522132.1:p.Ala606Pro
|
|
XM_024450741.1:c.1906G>C
|
XP_024306509.1:p.Ala636Pro
|
|
XR_934021.2:n.1973G>C
|
|
|
XR_934022.2:n.1879G>C
|
|
|
XR_934023.2:n.1900G>C
|
|
|
NM_000018.4:c.1918G>C
MANE Select
|
NP_000009.1:p.Ala640Pro
|
|
NM_001033859.3:c.1852G>C
|
NP_001029031.1:p.Ala618Pro
|
|
NM_001270447.2:c.1987G>C
|
NP_001257376.1:p.Ala663Pro
|
|
NM_001270448.2:c.1690G>C
|
NP_001257377.1:p.Ala564Pro
|
|