ENST00000261609.13:c.11960C>A
MANE Select
|
ENSP00000261609.8:p.Pro3987His
|
|
ENST00000650509.1:c.3671C>A
|
ENSP00000496936.1:p.Pro1224His
|
|
ENST00000261609.11:c.11960C>A
|
ENSP00000261609.7:p.Pro3987His
|
|
NM_004667.5:c.11960C>A
|
NP_004658.3:p.Pro3987His
|
|
XM_005268276.3:c.11846C>A
|
XP_005268333.1:p.Pro3949His
|
|
XM_005268277.3:c.11846C>A
|
XP_005268334.1:p.Pro3949His
|
|
XM_006720726.2:c.11945C>A
|
XP_006720789.1:p.Pro3982His
|
|
XM_006720727.2:c.11702C>A
|
XP_006720790.1:p.Pro3901His
|
|
XM_011522131.1:c.11477C>A
|
XP_011520433.1:p.Pro3826His
|
|
XM_011522132.1:c.9476C>A
|
XP_011520434.1:p.Pro3159His
|
|
XM_011522133.1:c.8705C>A
|
XP_011520435.1:p.Pro2902His
|
|
XM_011522134.1:c.6077C>A
|
XP_011520436.1:p.Pro2026His
|
|
XM_005268276.5:c.11846C>A
|
XP_005268333.1:p.Pro3949His
|
|
XM_006720726.3:c.11945C>A
|
XP_006720789.1:p.Pro3982His
|
|
XM_006720727.3:c.11702C>A
|
XP_006720790.1:p.Pro3901His
|
|
XM_017022695.1:c.11846C>A
|
XP_016878184.1:p.Pro3949His
|
|
XM_017022696.1:c.11846C>A
|
XP_016878185.1:p.Pro3949His
|
|
XM_017022697.1:c.5126C>A
|
XP_016878186.1:p.Pro1709His
|
|
XM_017022698.1:c.5126C>A
|
XP_016878187.1:p.Pro1709His
|
|
NM_004667.6:c.11960C>A
MANE Select
|
NP_004658.3:p.Pro3987His
|
|