ENST00000261609.13:c.11716C>A
MANE Select
|
ENSP00000261609.8:p.Arg3906Ser
|
|
ENST00000650509.1:c.3427C>A
|
ENSP00000496936.1:p.Arg1143Ser
|
|
ENST00000261609.11:c.11716C>A
|
ENSP00000261609.7:p.Arg3906Ser
|
|
ENST00000564519.1:n.231C>A
|
|
|
NM_004667.5:c.11716C>A
|
NP_004658.3:p.Arg3906Ser
|
|
XM_005268276.3:c.11602C>A
|
XP_005268333.1:p.Arg3868Ser
|
|
XM_005268277.3:c.11602C>A
|
XP_005268334.1:p.Arg3868Ser
|
|
XM_006720726.2:c.11701C>A
|
XP_006720789.1:p.Arg3901Ser
|
|
XM_006720727.2:c.11458C>A
|
XP_006720790.1:p.Arg3820Ser
|
|
XM_011522131.1:c.11233C>A
|
XP_011520433.1:p.Arg3745Ser
|
|
XM_011522132.1:c.9232C>A
|
XP_011520434.1:p.Arg3078Ser
|
|
XM_011522133.1:c.8461C>A
|
XP_011520435.1:p.Arg2821Ser
|
|
XM_011522134.1:c.5833C>A
|
XP_011520436.1:p.Arg1945Ser
|
|
XM_005268276.5:c.11602C>A
|
XP_005268333.1:p.Arg3868Ser
|
|
XM_006720726.3:c.11701C>A
|
XP_006720789.1:p.Arg3901Ser
|
|
XM_006720727.3:c.11458C>A
|
XP_006720790.1:p.Arg3820Ser
|
|
XM_017022695.1:c.11602C>A
|
XP_016878184.1:p.Arg3868Ser
|
|
XM_017022696.1:c.11602C>A
|
XP_016878185.1:p.Arg3868Ser
|
|
XM_017022697.1:c.4882C>A
|
XP_016878186.1:p.Arg1628Ser
|
|
XM_017022698.1:c.4882C>A
|
XP_016878187.1:p.Arg1628Ser
|
|
NM_004667.6:c.11716C>A
MANE Select
|
NP_004658.3:p.Arg3906Ser
|
|