|
NM_000203.5:c.1041C>G
MANE Select
|
NP_000194.2:p.Ser347Arg
|
|
ENST00000514224.2:c.1041C>G
MANE Select
|
ENSP00000425081.2:p.Ser347Arg
|
|
NM_000203.4:c.1041C>G
|
NP_000194.2:p.Ser347Arg
|
|
NM_001363576.1:c.645C>G
|
NP_001350505.1:p.Ser215Arg
|
|
NR_110313.1:n.1129C>G
|
|
|
ENST00000247933.8:c.1041C>G
|
ENSP00000247933.4:p.Ser347Arg
|
|
ENST00000247933.9:c.1041C>G
|
ENSP00000247933.4:p.Ser347Arg
|
|
ENST00000514224.1:c.645C>G
|
ENSP00000425081.1:p.Ser215Arg
|
|
ENST00000514698.5:n.1148C>G
|
|
|
ENST00000652070.1:n.1097C>G
|
|
|
XM_006713882.2:c.645C>G
|
XP_006713945.1:p.Ser215Arg
|
|
XM_011513459.1:c.1107C>G
|
XP_011511761.1:p.Ser369Arg
|
|
XM_011513460.1:c.900C>G
|
XP_011511762.1:p.Ser300Arg
|
|
XM_011513461.1:c.834C>G
|
XP_011511763.1:p.Ser278Arg
|
|
XM_011513461.2:c.834C>G
|
XP_011511763.1:p.Ser278Arg
|
|
XM_011513462.1:c.753C>G
|
XP_011511764.1:p.Ser251Arg
|
|
XM_011513463.1:c.753C>G
|
XP_011511765.1:p.Ser251Arg
|
|
XM_017008163.1:c.81C>G
|
XP_016863652.1:p.Ser27Arg
|
|
XR_924947.1:n.1110C>G
|
|