ENST00000647956.2:c.187T=
(C1R)
MANE Select
|
ENSP00000497341.1:p.Phe63=
|
|
ENST00000535233.6:c.187T=
(C1R)
|
ENSP00000438636.3:p.Phe63=
|
|
ENST00000536053.6:c.229T=
(C1R)
|
ENSP00000444271.3:p.Phe77=
|
|
ENST00000536092.1:n.292T=
(C1R)
|
|
|
ENST00000538050.5:c.-129T=
(C1R)
|
ENSP00000444009.1:n.-129T=
|
|
ENST00000539803.5:c.654T=
(C1RL)
|
|
|
ENST00000540242.2:c.187T=
(C1R)
|
ENSP00000442946.1:p.Phe63=
|
|
ENST00000540394.5:n.946T=
(C1R)
|
|
|
ENST00000540610.5:c.-85+891T=
(C1R)
|
ENSP00000439223.1:n.-85+891T=
|
|
ENST00000541042.5:c.-129T=
(C1R)
|
ENSP00000441601.1:n.-129T=
|
|
ENST00000542285.5:c.187T=
(C1R)
|
ENSP00000438615.2:p.Phe63=
|
|
ENST00000543362.5:c.187T=
(C1R)
|
ENSP00000446356.1:p.Phe63=
|
|
ENST00000543835.5:c.187T=
(C1R)
|
ENSP00000445285.1:p.Phe63=
|
|
ENST00000545466.1:n.240T=
(C1R)
|
|
|
NM_001733.4:c.187T=
(C1R)
|
NP_001724.3:p.Phe63=
|
|
NM_001354346.1:c.229T=
(C1R)
|
NP_001341275.1:p.Phe77=
|
|
NM_001733.6:c.187T=
(C1R)
|
NP_001724.4:p.Phe63=
|
|
NM_001733.7:c.187T=
(C1R)
MANE Select
|
NP_001724.4:p.Phe63=
|
|
NM_001354346.2:c.229T=
(C1R)
|
NP_001341275.1:p.Phe77=
|
|