ENST00000394249.8:c.*506T>A
(PRC1)
MANE Select
|
ENSP00000377793.3:n.*506T>A
|
|
ENST00000643536.1:c.*4131T>A
|
ENSP00000494429.1:n.*4131T>A
|
|
ENST00000361188.9:c.*506T>A
(PRC1)
|
ENSP00000354679.5:n.*506T>A
|
|
ENST00000394249.7:c.*506T>A
(PRC1)
|
ENSP00000377793.3:n.*506T>A
|
|
ENST00000555455.5:c.670T>A
(PRC1)
|
|
|
ENST00000556972.6:c.153T>A
(PRC1)
|
ENSP00000456737.1:n.153T>A
|
|
NM_001267580.1:c.*549T>A
(PRC1)
|
NP_001254509.1:n.*549T>A
|
|
NM_003981.3:c.*506T>A
(PRC1)
|
NP_003972.1:n.*506T>A
|
|
NM_199413.2:c.*506T>A
(PRC1)
|
NP_955445.1:n.*506T>A
|
|
NR_051984.1:n.257A>T
(PRC1-AS1)
|
|
|
XM_005254987.1:c.*549T>A
(PRC1)
|
XP_005255044.1:n.*549T>A
|
|
XM_006720759.1:c.*600T>A
(PRC1)
|
XP_006720822.1:n.*600T>A
|
|
XM_006720760.1:c.*12T>A
(PRC1)
|
XP_006720823.1:n.*12T>A
|
|
XM_011522187.1:c.1820T>A
(PRC1)
|
XP_011520489.1:p.Phe607Tyr
|
|
XM_011522188.1:c.1778T>A
(PRC1)
|
XP_011520490.1:p.Phe593Tyr
|
|
XM_011522189.1:c.1709T>A
(PRC1)
|
XP_011520491.1:p.Phe570Tyr
|
|
XM_011522190.1:c.1649T>A
(PRC1)
|
XP_011520492.1:p.Phe550Tyr
|
|
XM_011522191.1:c.*51T>A
(PRC1)
|
XP_011520493.1:n.*51T>A
|
|
XM_011522192.1:c.1499T>A
(PRC1)
|
XP_011520494.1:p.Phe500Tyr
|
|
XM_005254987.3:c.*549T>A
(PRC1)
|
XP_005255044.1:n.*549T>A
|
|
XM_006720759.2:c.*600T>A
(PRC1)
|
XP_006720822.1:n.*600T>A
|
|
XM_006720760.2:c.*12T>A
(PRC1)
|
XP_006720823.1:n.*12T>A
|
|
XM_011522187.2:c.1820T>A
(PRC1)
|
XP_011520489.1:p.Phe607Tyr
|
|
XM_011522188.3:c.1778T>A
(PRC1)
|
XP_011520490.1:p.Phe593Tyr
|
|
XM_011522189.2:c.1709T>A
(PRC1)
|
XP_011520491.1:p.Phe570Tyr
|
|
XM_011522190.3:c.1649T>A
(PRC1)
|
XP_011520492.1:p.Phe550Tyr
|
|
XM_011522191.3:c.*51T>A
(PRC1)
|
XP_011520493.1:n.*51T>A
|
|
XM_011522192.2:c.1499T>A
(PRC1)
|
XP_011520494.1:p.Phe500Tyr
|
|
XM_017022712.2:c.*506T>A
(PRC1)
|
XP_016878201.1:n.*506T>A
|
|
XM_017022713.2:c.*506T>A
(PRC1)
|
XP_016878202.1:n.*506T>A
|
|
XM_017022714.2:c.1664T>A
(PRC1)
|
XP_016878203.1:p.Phe555Tyr
|
|
XM_017022715.2:c.*506T>A
(PRC1)
|
XP_016878204.1:n.*506T>A
|
|
XM_017022716.2:c.*506T>A
(PRC1)
|
XP_016878205.1:n.*506T>A
|
|
XM_017022717.1:c.*549T>A
(PRC1)
|
XP_016878206.1:n.*549T>A
|
|
NM_003981.4:c.*506T>A
(PRC1)
MANE Select
|
NP_003972.2:n.*506T>A
|
|
NM_001267580.2:c.*549T>A
(PRC1)
|
NP_001254509.2:n.*549T>A
|
|
NM_199413.3:c.*506T>A
(PRC1)
|
NP_955445.2:n.*506T>A
|
|