ENST00000261609.13:c.11718T>A
MANE Select
|
ENSP00000261609.8:p.Arg3906=
|
|
ENST00000650509.1:c.3429T>A
|
ENSP00000496936.1:p.Arg1143=
|
|
ENST00000261609.11:c.11718T>A
|
ENSP00000261609.7:p.Arg3906=
|
|
ENST00000564519.1:n.233T>A
|
|
|
NM_004667.5:c.11718T>A
|
NP_004658.3:p.Arg3906=
|
|
XM_005268276.3:c.11604T>A
|
XP_005268333.1:p.Arg3868=
|
|
XM_005268277.3:c.11604T>A
|
XP_005268334.1:p.Arg3868=
|
|
XM_006720726.2:c.11703T>A
|
XP_006720789.1:p.Arg3901=
|
|
XM_006720727.2:c.11460T>A
|
XP_006720790.1:p.Arg3820=
|
|
XM_011522131.1:c.11235T>A
|
XP_011520433.1:p.Arg3745=
|
|
XM_011522132.1:c.9234T>A
|
XP_011520434.1:p.Arg3078=
|
|
XM_011522133.1:c.8463T>A
|
XP_011520435.1:p.Arg2821=
|
|
XM_011522134.1:c.5835T>A
|
XP_011520436.1:p.Arg1945=
|
|
XM_005268276.5:c.11604T>A
|
XP_005268333.1:p.Arg3868=
|
|
XM_006720726.3:c.11703T>A
|
XP_006720789.1:p.Arg3901=
|
|
XM_006720727.3:c.11460T>A
|
XP_006720790.1:p.Arg3820=
|
|
XM_017022695.1:c.11604T>A
|
XP_016878184.1:p.Arg3868=
|
|
XM_017022696.1:c.11604T>A
|
XP_016878185.1:p.Arg3868=
|
|
XM_017022697.1:c.4884T>A
|
XP_016878186.1:p.Arg1628=
|
|
XM_017022698.1:c.4884T>A
|
XP_016878187.1:p.Arg1628=
|
|
NM_004667.6:c.11718T>A
MANE Select
|
NP_004658.3:p.Arg3906=
|
|