ENST00000394249.8:c.*498G>T
(PRC1)
MANE Select
|
ENSP00000377793.3:n.*498G>T
|
|
ENST00000643536.1:c.*4123G>T
|
ENSP00000494429.1:n.*4123G>T
|
|
ENST00000361188.9:c.*498G>T
(PRC1)
|
ENSP00000354679.5:n.*498G>T
|
|
ENST00000394249.7:c.*498G>T
(PRC1)
|
ENSP00000377793.3:n.*498G>T
|
|
ENST00000555455.5:c.662G>T
(PRC1)
|
|
|
ENST00000556972.6:c.145G>T
(PRC1)
|
ENSP00000456737.1:n.145G>T
|
|
NM_001267580.1:c.*541G>T
(PRC1)
|
NP_001254509.1:n.*541G>T
|
|
NM_003981.3:c.*498G>T
(PRC1)
|
NP_003972.1:n.*498G>T
|
|
NM_199413.2:c.*498G>T
(PRC1)
|
NP_955445.1:n.*498G>T
|
|
NR_051984.1:n.265C>A
(PRC1-AS1)
|
|
|
XM_005254987.1:c.*541G>T
(PRC1)
|
XP_005255044.1:n.*541G>T
|
|
XM_006720759.1:c.*592G>T
(PRC1)
|
XP_006720822.1:n.*592G>T
|
|
XM_006720760.1:c.*4G>T
(PRC1)
|
XP_006720823.1:n.*4G>T
|
|
XM_011522187.1:c.1812G>T
(PRC1)
|
XP_011520489.1:p.Glu604Asp
|
|
XM_011522188.1:c.1770G>T
(PRC1)
|
XP_011520490.1:p.Glu590Asp
|
|
XM_011522189.1:c.1701G>T
(PRC1)
|
XP_011520491.1:p.Glu567Asp
|
|
XM_011522190.1:c.1641G>T
(PRC1)
|
XP_011520492.1:p.Glu547Asp
|
|
XM_011522191.1:c.*43G>T
(PRC1)
|
XP_011520493.1:n.*43G>T
|
|
XM_011522192.1:c.1491G>T
(PRC1)
|
XP_011520494.1:p.Glu497Asp
|
|
XM_005254987.3:c.*541G>T
(PRC1)
|
XP_005255044.1:n.*541G>T
|
|
XM_006720759.2:c.*592G>T
(PRC1)
|
XP_006720822.1:n.*592G>T
|
|
XM_006720760.2:c.*4G>T
(PRC1)
|
XP_006720823.1:n.*4G>T
|
|
XM_011522187.2:c.1812G>T
(PRC1)
|
XP_011520489.1:p.Glu604Asp
|
|
XM_011522188.3:c.1770G>T
(PRC1)
|
XP_011520490.1:p.Glu590Asp
|
|
XM_011522189.2:c.1701G>T
(PRC1)
|
XP_011520491.1:p.Glu567Asp
|
|
XM_011522190.3:c.1641G>T
(PRC1)
|
XP_011520492.1:p.Glu547Asp
|
|
XM_011522191.3:c.*43G>T
(PRC1)
|
XP_011520493.1:n.*43G>T
|
|
XM_011522192.2:c.1491G>T
(PRC1)
|
XP_011520494.1:p.Glu497Asp
|
|
XM_017022712.2:c.*498G>T
(PRC1)
|
XP_016878201.1:n.*498G>T
|
|
XM_017022713.2:c.*498G>T
(PRC1)
|
XP_016878202.1:n.*498G>T
|
|
XM_017022714.2:c.1656G>T
(PRC1)
|
XP_016878203.1:p.Glu552Asp
|
|
XM_017022715.2:c.*498G>T
(PRC1)
|
XP_016878204.1:n.*498G>T
|
|
XM_017022716.2:c.*498G>T
(PRC1)
|
XP_016878205.1:n.*498G>T
|
|
XM_017022717.1:c.*541G>T
(PRC1)
|
XP_016878206.1:n.*541G>T
|
|
NM_003981.4:c.*498G>T
(PRC1)
MANE Select
|
NP_003972.2:n.*498G>T
|
|
NM_001267580.2:c.*541G>T
(PRC1)
|
NP_001254509.2:n.*541G>T
|
|
NM_199413.3:c.*498G>T
(PRC1)
|
NP_955445.2:n.*498G>T
|
|