ENST00000372236.9:c.351T>G
(POLH)
MANE Select
|
ENSP00000361310.4:p.Ala117=
|
|
ENST00000372226.1:c.351T>G
(POLH)
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ENSP00000361300.1:p.Ala117=
|
|
ENST00000372236.8:c.351T>G
(POLH)
|
ENSP00000361310.4:p.Ala117=
|
|
ENST00000443535.1:c.165T>G
(POLH)
|
ENSP00000405320.1:p.Ala55=
|
|
NM_001291969.1:c.118+4209T>G
(POLH)
|
NP_001278898.1:n.118+4209T>G
|
|
NM_001291970.1:c.351T>G
(POLH)
|
NP_001278899.1:p.Ala117=
|
|
NM_006502.2:c.351T>G , LRG_470t1:c.351T>G
(POLH)
|
NP_006493.1:p.Ala117=
|
|
XM_005249186.2:c.165T>G
(POLH)
|
XP_005249243.1:p.Ala55=
|
|
XM_011514698.1:c.118+4209T>G
(POLH)
|
XP_011513000.1:n.118+4209T>G
|
|
XM_005249186.4:c.165T>G
(POLH)
|
XP_005249243.1:p.Ala55=
|
|
XM_011514698.3:c.118+4209T>G
(POLH)
|
XP_011513000.1:n.118+4209T>G
|
|
XM_024446466.1:c.99T>G
(POLH)
|
XP_024302234.1:p.Ala33=
|
|
XM_024446467.1:c.-269T>G
(POLH)
|
XP_024302235.1:n.-269T>G
|
|
NM_001291969.2:c.118+4209T>G
(POLH)
|
NP_001278898.1:n.118+4209T>G
|
|
NM_001291970.2:c.351T>G
(POLH)
|
NP_001278899.1:p.Ala117=
|
|
NM_006502.3:c.351T>G
(POLH)
MANE Select
|
NP_006493.1:p.Ala117=
|
|
NM_001318876.2:c.945+58079T>G
(POLR1C)
|
NP_001305805.1:n.945+58079T>G
|
|