|
NM_001278055.1:c.9472A>C
|
NP_001264984.1:p.Ser3158Arg
|
|
|
NM_014363.5:c.9913A>C
|
NP_055178.3:p.Ser3305Arg
|
|
|
XM_005266338.1:c.9940A>C
|
XP_005266395.1:p.Ser3314Arg
|
|
|
XM_011535038.1:c.9964A>C
|
XP_011533340.1:p.Ser3322Arg
|
|
|
XM_011535039.1:c.9931A>C
|
XP_011533341.1:p.Ser3311Arg
|
|
|
XM_005266338.2:c.9940A>C
|
XP_005266395.1:p.Ser3314Arg
|
|
|
XM_011535039.2:c.9931A>C
|
XP_011533341.1:p.Ser3311Arg
|
|
|
XM_017020539.1:c.9904A>C
|
XP_016876028.1:p.Ser3302Arg
|
|
|
XM_024449337.1:c.9940A>C
|
XP_024305105.1:p.Ser3314Arg
|
|
|
NM_014363.6:c.9913A>C
MANE Select
|
NP_055178.3:p.Ser3305Arg
|
|
|
NM_001278055.2:c.9472A>C
|
NP_001264984.1:p.Ser3158Arg
|
|
|
ENST00000382292.7:c.9913A>C
|
ENSP00000371729.3:p.Ser3305Arg
|
|
|
ENST00000382298.7:c.9913A>C
|
ENSP00000371735.3:p.Ser3305Arg
|
|
|
ENST00000402364.1:c.7663A>C
|
ENSP00000385844.1:p.Ser2555Arg
|
|
|
ENST00000423156.1:n.1058-4479A>C
|
ENSP00000390925.1:p.=
|
|
|
ENST00000455470.5:n.2130-4479A>C
|
|
|
