ENST00000261609.13:c.11934C>A
MANE Select
|
ENSP00000261609.8:p.Pro3978=
|
|
ENST00000650509.1:c.3645C>A
|
ENSP00000496936.1:p.Pro1215=
|
|
ENST00000261609.11:c.11934C>A
|
ENSP00000261609.7:p.Pro3978=
|
|
NM_004667.5:c.11934C>A
|
NP_004658.3:p.Pro3978=
|
|
XM_005268276.3:c.11820C>A
|
XP_005268333.1:p.Pro3940=
|
|
XM_005268277.3:c.11820C>A
|
XP_005268334.1:p.Pro3940=
|
|
XM_006720726.2:c.11919C>A
|
XP_006720789.1:p.Pro3973=
|
|
XM_006720727.2:c.11676C>A
|
XP_006720790.1:p.Pro3892=
|
|
XM_011522131.1:c.11451C>A
|
XP_011520433.1:p.Pro3817=
|
|
XM_011522132.1:c.9450C>A
|
XP_011520434.1:p.Pro3150=
|
|
XM_011522133.1:c.8679C>A
|
XP_011520435.1:p.Pro2893=
|
|
XM_011522134.1:c.6051C>A
|
XP_011520436.1:p.Pro2017=
|
|
XM_005268276.5:c.11820C>A
|
XP_005268333.1:p.Pro3940=
|
|
XM_006720726.3:c.11919C>A
|
XP_006720789.1:p.Pro3973=
|
|
XM_006720727.3:c.11676C>A
|
XP_006720790.1:p.Pro3892=
|
|
XM_017022695.1:c.11820C>A
|
XP_016878184.1:p.Pro3940=
|
|
XM_017022696.1:c.11820C>A
|
XP_016878185.1:p.Pro3940=
|
|
XM_017022697.1:c.5100C>A
|
XP_016878186.1:p.Pro1700=
|
|
XM_017022698.1:c.5100C>A
|
XP_016878187.1:p.Pro1700=
|
|
NM_004667.6:c.11934C>A
MANE Select
|
NP_004658.3:p.Pro3978=
|
|