ENST00000710953.1:c.*2081C>A
(ERCC1)
|
ENSP00000518553.1:n.*2081C>A
|
|
ENST00000300853.8:c.*1848C>A
(ERCC1)
MANE Select
|
ENSP00000300853.3:n.*1848C>A
|
|
ENST00000309424.8:c.165-306G>T
(POLR1G)
MANE Select
|
ENSP00000310966.3:n.165-306G>T
|
|
ENST00000300853.7:c.*1848C>A
(ERCC1)
|
ENSP00000300853.2:n.*1848C>A
|
|
ENST00000309424.7:c.165-306G>T
(POLR1G)
|
ENSP00000310966.3:n.165-306G>T
|
|
ENST00000423698.6:c.*1848C>A
(ERCC1)
|
ENSP00000394875.2:n.*1848C>A
|
|
ENST00000589804.1:c.171-306G>T
(POLR1G)
|
ENSP00000465099.1:n.171-306G>T
|
|
ENST00000590794.1:c.21-306G>T
(POLR1G)
|
|
|
ENST00000592852.1:c.-370-306G>T
(POLR1G)
|
ENSP00000467771.1:n.-370-306G>T
|
|
NM_001166049.1:c.*1848C>A
(ERCC1)
|
NP_001159521.1:n.*1848C>A
|
|
NM_001297590.1:c.171-306G>T
(POLR1G)
|
NP_001284519.1:n.171-306G>T
|
|
NM_001983.3:c.*1848C>A
(ERCC1)
|
NP_001974.1:n.*1848C>A
|
|
NM_012099.1:c.165-306G>T
(POLR1G)
|
NP_036231.1:n.165-306G>T
|
|
XM_017026460.2:c.*1848C>A
(ERCC1)
|
XP_016881949.1:n.*1848C>A
|
|
XM_017026461.1:c.*1848C>A
(ERCC1)
|
XP_016881950.1:n.*1848C>A
|
|
XM_017026462.1:c.*1848C>A
(ERCC1)
|
XP_016881951.1:n.*1848C>A
|
|
XM_017026463.1:c.*1848C>A
(ERCC1)
|
XP_016881952.1:n.*1848C>A
|
|
XM_017026464.1:c.*1848C>A
(ERCC1)
|
XP_016881953.1:n.*1848C>A
|
|
XM_017026465.1:c.*1848C>A
(ERCC1)
|
XP_016881954.1:n.*1848C>A
|
|
XM_017026466.1:c.*1848C>A
(ERCC1)
|
XP_016881955.1:n.*1848C>A
|
|
XR_001753631.1:n.3328C>A
(ERCC1)
|
|
|
XR_001753632.1:n.3798C>A
(ERCC1)
|
|
|
NM_001166049.2:c.*1848C>A
(ERCC1)
|
NP_001159521.1:n.*1848C>A
|
|
NM_001297590.2:c.171-306G>T
(POLR1G)
|
NP_001284519.1:n.171-306G>T
|
|
NM_001369412.1:c.*1848C>A
(ERCC1)
|
NP_001356341.1:n.*1848C>A
|
|
NM_001369413.1:c.*1848C>A
(ERCC1)
|
NP_001356342.1:n.*1848C>A
|
|
NM_001369414.1:c.*1848C>A
(ERCC1)
|
NP_001356343.1:n.*1848C>A
|
|
NM_001369415.1:c.*1848C>A
(ERCC1)
|
NP_001356344.1:n.*1848C>A
|
|
NM_001369416.1:c.*1848C>A
(ERCC1)
|
NP_001356345.1:n.*1848C>A
|
|
NM_001369417.1:c.*1848C>A
(ERCC1)
|
NP_001356346.1:n.*1848C>A
|
|
NM_001369418.1:c.*1848C>A
(ERCC1)
|
NP_001356347.1:n.*1848C>A
|
|
NM_001369419.1:c.*1848C>A
(ERCC1)
|
NP_001356348.1:n.*1848C>A
|
|
NM_001983.4:c.*1848C>A
(ERCC1)
MANE Select
|
NP_001974.1:n.*1848C>A
|
|
NM_012099.2:c.165-306G>T
(POLR1G)
|
NP_036231.1:n.165-306G>T
|
|
NM_001297590.3:c.171-306G>T
(POLR1G)
|
NP_001284519.1:n.171-306G>T
|
|
NM_012099.3:c.165-306G>T
(POLR1G)
MANE Select
|
NP_036231.1:n.165-306G>T
|
|