ENST00000261609.13:c.11928C>G
MANE Select
|
ENSP00000261609.8:p.Pro3976=
|
|
ENST00000650509.1:c.3639C>G
|
ENSP00000496936.1:p.Pro1213=
|
|
ENST00000261609.11:c.11928C>G
|
ENSP00000261609.7:p.Pro3976=
|
|
NM_004667.5:c.11928C>G
|
NP_004658.3:p.Pro3976=
|
|
XM_005268276.3:c.11814C>G
|
XP_005268333.1:p.Pro3938=
|
|
XM_005268277.3:c.11814C>G
|
XP_005268334.1:p.Pro3938=
|
|
XM_006720726.2:c.11913C>G
|
XP_006720789.1:p.Pro3971=
|
|
XM_006720727.2:c.11670C>G
|
XP_006720790.1:p.Pro3890=
|
|
XM_011522131.1:c.11445C>G
|
XP_011520433.1:p.Pro3815=
|
|
XM_011522132.1:c.9444C>G
|
XP_011520434.1:p.Pro3148=
|
|
XM_011522133.1:c.8673C>G
|
XP_011520435.1:p.Pro2891=
|
|
XM_011522134.1:c.6045C>G
|
XP_011520436.1:p.Pro2015=
|
|
XM_005268276.5:c.11814C>G
|
XP_005268333.1:p.Pro3938=
|
|
XM_006720726.3:c.11913C>G
|
XP_006720789.1:p.Pro3971=
|
|
XM_006720727.3:c.11670C>G
|
XP_006720790.1:p.Pro3890=
|
|
XM_017022695.1:c.11814C>G
|
XP_016878184.1:p.Pro3938=
|
|
XM_017022696.1:c.11814C>G
|
XP_016878185.1:p.Pro3938=
|
|
XM_017022697.1:c.5094C>G
|
XP_016878186.1:p.Pro1698=
|
|
XM_017022698.1:c.5094C>G
|
XP_016878187.1:p.Pro1698=
|
|
NM_004667.6:c.11928C>G
MANE Select
|
NP_004658.3:p.Pro3976=
|
|