ENST00000261609.13:c.11772T>G
MANE Select
|
ENSP00000261609.8:p.Ile3924Met
|
|
ENST00000650509.1:c.3483T>G
|
ENSP00000496936.1:p.Ile1161Met
|
|
ENST00000261609.11:c.11772T>G
|
ENSP00000261609.7:p.Ile3924Met
|
|
ENST00000564519.1:n.287T>G
|
|
|
NM_004667.5:c.11772T>G
|
NP_004658.3:p.Ile3924Met
|
|
XM_005268276.3:c.11658T>G
|
XP_005268333.1:p.Ile3886Met
|
|
XM_005268277.3:c.11658T>G
|
XP_005268334.1:p.Ile3886Met
|
|
XM_006720726.2:c.11757T>G
|
XP_006720789.1:p.Ile3919Met
|
|
XM_006720727.2:c.11514T>G
|
XP_006720790.1:p.Ile3838Met
|
|
XM_011522131.1:c.11289T>G
|
XP_011520433.1:p.Ile3763Met
|
|
XM_011522132.1:c.9288T>G
|
XP_011520434.1:p.Ile3096Met
|
|
XM_011522133.1:c.8517T>G
|
XP_011520435.1:p.Ile2839Met
|
|
XM_011522134.1:c.5889T>G
|
XP_011520436.1:p.Ile1963Met
|
|
XM_005268276.5:c.11658T>G
|
XP_005268333.1:p.Ile3886Met
|
|
XM_006720726.3:c.11757T>G
|
XP_006720789.1:p.Ile3919Met
|
|
XM_006720727.3:c.11514T>G
|
XP_006720790.1:p.Ile3838Met
|
|
XM_017022695.1:c.11658T>G
|
XP_016878184.1:p.Ile3886Met
|
|
XM_017022696.1:c.11658T>G
|
XP_016878185.1:p.Ile3886Met
|
|
XM_017022697.1:c.4938T>G
|
XP_016878186.1:p.Ile1646Met
|
|
XM_017022698.1:c.4938T>G
|
XP_016878187.1:p.Ile1646Met
|
|
NM_004667.6:c.11772T>G
MANE Select
|
NP_004658.3:p.Ile3924Met
|
|