ENST00000397088.4:c.*679G>A
(GPER1)
MANE Select
|
ENSP00000380277.3:n.*679G>A
|
|
ENST00000397098.8:c.129+33722C>T
(C7orf50)
MANE Select
|
ENSP00000380286.3:n.129+33722C>T
|
|
ENST00000297469.3:c.*679G>A
(GPER1)
|
ENSP00000297469.3:n.*679G>A
|
|
ENST00000357429.10:c.129+33722C>T
(C7orf50)
|
ENSP00000350011.5:n.129+33722C>T
|
|
ENST00000397088.3:c.*679G>A
(GPER1)
|
ENSP00000380277.3:n.*679G>A
|
|
ENST00000397092.5:c.*679G>A
(GPER1)
|
ENSP00000380281.1:n.*679G>A
|
|
ENST00000397098.7:c.129+33722C>T
(C7orf50)
|
ENSP00000380286.3:n.129+33722C>T
|
|
ENST00000397100.6:c.129+33722C>T
(C7orf50)
|
ENSP00000380288.2:n.129+33722C>T
|
|
ENST00000488073.1:n.266+15793C>T
(C7orf50)
|
|
|
ENST00000491163.1:c.129+33722C>T
(C7orf50)
|
ENSP00000420130.1:n.129+33722C>T
|
|
ENST00000617001.1:c.*298G>A
(GPER1)
|
ENSP00000479553.1:n.*298G>A
|
|
ENST00000619052.1:c.365G>A
(GPER1)
|
ENSP00000483756.1:p.Arg122His
|
|
NM_001039966.1:c.*679G>A
(GPER1)
|
NP_001035055.1:n.*679G>A
|
|
NM_001098201.1:c.*679G>A
(GPER1)
|
NP_001091671.1:n.*679G>A
|
|
NM_001134395.1:c.129+33722C>T
(C7orf50)
|
NP_001127867.1:n.129+33722C>T
|
|
NM_001134396.1:c.129+33722C>T
(C7orf50)
|
NP_001127868.1:n.129+33722C>T
|
|
NM_001505.2:c.*679G>A
(GPER1)
|
NP_001496.1:n.*679G>A
|
|
NM_032350.5:c.129+33722C>T
(C7orf50)
|
NP_115726.1:n.129+33722C>T
|
|
XM_005249888.3:c.129+33722C>T
(C7orf50)
|
XP_005249945.1:n.129+33722C>T
|
|
XM_011515581.1:c.129+33722C>T
(C7orf50)
|
XP_011513883.1:n.129+33722C>T
|
|
XM_011515582.1:c.129+33722C>T
(C7orf50)
|
XP_011513884.1:n.129+33722C>T
|
|
XM_011515583.1:c.129+33722C>T
(C7orf50)
|
XP_011513885.1:n.129+33722C>T
|
|
XM_011515584.1:c.129+33722C>T
(C7orf50)
|
XP_011513886.1:n.129+33722C>T
|
|
NM_001098201.2:c.*679G>A
(GPER1)
|
NP_001091671.1:n.*679G>A
|
|
NM_001318252.1:c.129+33722C>T
(C7orf50)
|
NP_001305181.1:n.129+33722C>T
|
|
NM_001350968.1:c.129+33722C>T
(C7orf50)
|
NP_001337897.1:n.129+33722C>T
|
|
XM_011515581.3:c.129+33722C>T
(C7orf50)
|
XP_011513883.1:n.129+33722C>T
|
|
XM_011515582.3:c.129+33722C>T
(C7orf50)
|
XP_011513884.1:n.129+33722C>T
|
|
XM_011515583.2:c.129+33722C>T
(C7orf50)
|
XP_011513885.1:n.129+33722C>T
|
|
XM_011515584.2:c.129+33722C>T
(C7orf50)
|
XP_011513886.1:n.129+33722C>T
|
|
XM_017012720.2:c.129+33722C>T
(C7orf50)
|
XP_016868209.1:n.129+33722C>T
|
|
XM_017012721.2:c.-145+33722C>T
(C7orf50)
|
XP_016868210.1:n.-145+33722C>T
|
|
XM_024446977.1:c.129+33722C>T
(C7orf50)
|
XP_024302745.1:n.129+33722C>T
|
|
XM_024446978.1:c.-145+33722C>T
(C7orf50)
|
XP_024302746.1:n.-145+33722C>T
|
|
NM_001098201.3:c.*679G>A
(GPER1)
MANE Select
|
NP_001091671.1:n.*679G>A
|
|
NM_001318252.2:c.129+33722C>T
(C7orf50)
MANE Select
|
NP_001305181.1:n.129+33722C>T
|
|
NM_001505.3:c.*679G>A
(GPER1)
|
NP_001496.1:n.*679G>A
|
|
NM_001039966.2:c.*679G>A
(GPER1)
|
NP_001035055.1:n.*679G>A
|
|