ENST00000356839.10:c.1929G>C
MANE Select
|
ENSP00000349297.5:p.Glu643Asp
|
|
ENST00000322910.9:c.*1884G>C
|
ENSP00000325395.5:n.*1884G>C
|
|
ENST00000350303.9:c.1863G>C
|
ENSP00000344152.5:p.Glu621Asp
|
|
ENST00000356839.9:c.1929G>C
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ENSP00000349297.5:p.Glu643Asp
|
|
ENST00000542255.6:c.808G>C
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|
|
ENST00000543245.6:c.1998G>C
|
ENSP00000438689.2:p.Glu666Asp
|
|
ENST00000578033.1:n.354G>C
|
|
|
ENST00000578319.5:n.510G>C
|
|
|
ENST00000578711.1:n.1554G>C
|
|
|
ENST00000578809.5:n.501G>C
|
|
|
ENST00000579425.5:n.1045G>C
|
|
|
ENST00000583848.5:c.295G>C
|
ENSP00000466487.1:n.295G>C
|
|
ENST00000583850.5:n.700G>C
|
|
|
ENST00000583858.5:c.860G>C
|
|
|
NM_000018.3:c.1929G>C
|
NP_000009.1:p.Glu643Asp
|
|
NM_001033859.2:c.1863G>C
|
NP_001029031.1:p.Glu621Asp
|
|
NM_001270447.1:c.1998G>C
|
NP_001257376.1:p.Glu666Asp
|
|
NM_001270448.1:c.1701G>C
|
NP_001257377.1:p.Glu567Asp
|
|
XM_006721516.2:c.1950G>C
|
XP_006721579.2:p.Glu650Asp
|
|
XM_011523829.1:c.1848G>C
|
XP_011522131.1:p.Glu616Asp
|
|
XM_011523830.1:c.1827G>C
|
XP_011522132.1:p.Glu609Asp
|
|
XR_934021.1:n.2032G>C
|
|
|
XR_934022.1:n.1938G>C
|
|
|
XR_934023.1:n.1959G>C
|
|
|
XM_006721516.3:c.1950G>C
|
XP_006721579.2:p.Glu650Asp
|
|
XM_011523829.2:c.1848G>C
|
XP_011522131.1:p.Glu616Asp
|
|
XM_011523830.2:c.1827G>C
|
XP_011522132.1:p.Glu609Asp
|
|
XM_024450741.1:c.1917G>C
|
XP_024306509.1:p.Glu639Asp
|
|
XR_934021.2:n.1984G>C
|
|
|
XR_934022.2:n.1890G>C
|
|
|
XR_934023.2:n.1911G>C
|
|
|
NM_000018.4:c.1929G>C
MANE Select
|
NP_000009.1:p.Glu643Asp
|
|
NM_001033859.3:c.1863G>C
|
NP_001029031.1:p.Glu621Asp
|
|
NM_001270447.2:c.1998G>C
|
NP_001257376.1:p.Glu666Asp
|
|
NM_001270448.2:c.1701G>C
|
NP_001257377.1:p.Glu567Asp
|
|