ENST00000247933.9:c.801C>G
|
ENSP00000247933.4:p.Arg267=
|
|
ENST00000514224.2:c.801C>G
MANE Select
|
ENSP00000425081.2:p.Arg267=
|
|
ENST00000652070.1:n.857C>G
|
|
|
ENST00000247933.8:c.801C>G
|
ENSP00000247933.4:p.Arg267=
|
|
ENST00000502910.5:c.660C>G
|
ENSP00000422952.1:p.Arg220=
|
|
ENST00000514192.5:c.618C>G
|
ENSP00000423685.1:p.Arg206=
|
|
ENST00000514224.1:c.405C>G
|
ENSP00000425081.1:p.Arg135=
|
|
ENST00000514698.5:n.801C>G
|
|
|
NM_000203.4:c.801C>G
|
NP_000194.2:p.Arg267=
|
|
NR_110313.1:n.889C>G
|
|
|
XM_006713882.2:c.405C>G
|
XP_006713945.1:p.Arg135=
|
|
XM_011513459.1:c.760C>G
|
XP_011511761.1:p.Gln254Glu
|
|
XM_011513460.1:c.660C>G
|
XP_011511762.1:p.Arg220=
|
|
XM_011513461.1:c.594C>G
|
XP_011511763.1:p.Arg198=
|
|
XM_011513462.1:c.513C>G
|
XP_011511764.1:p.Arg171=
|
|
XM_011513463.1:c.513C>G
|
XP_011511765.1:p.Arg171=
|
|
XR_924947.1:n.870C>G
|
|
|
NM_000203.5:c.801C>G
MANE Select
|
NP_000194.2:p.Arg267=
|
|
NM_001363576.1:c.405C>G
|
NP_001350505.1:p.Arg135=
|
|
XM_011513461.2:c.594C>G
|
XP_011511763.1:p.Arg198=
|
|
XM_017008163.1:c.-160C>G
|
XP_016863652.1:n.-160C>G
|
|