ENST00000261609.13:c.11727G>T
MANE Select
|
ENSP00000261609.8:p.Met3909Ile
|
|
ENST00000650509.1:c.3438G>T
|
ENSP00000496936.1:p.Met1146Ile
|
|
ENST00000261609.11:c.11727G>T
|
ENSP00000261609.7:p.Met3909Ile
|
|
ENST00000564519.1:n.242G>T
|
|
|
NM_004667.5:c.11727G>T
|
NP_004658.3:p.Met3909Ile
|
|
XM_005268276.3:c.11613G>T
|
XP_005268333.1:p.Met3871Ile
|
|
XM_005268277.3:c.11613G>T
|
XP_005268334.1:p.Met3871Ile
|
|
XM_006720726.2:c.11712G>T
|
XP_006720789.1:p.Met3904Ile
|
|
XM_006720727.2:c.11469G>T
|
XP_006720790.1:p.Met3823Ile
|
|
XM_011522131.1:c.11244G>T
|
XP_011520433.1:p.Met3748Ile
|
|
XM_011522132.1:c.9243G>T
|
XP_011520434.1:p.Met3081Ile
|
|
XM_011522133.1:c.8472G>T
|
XP_011520435.1:p.Met2824Ile
|
|
XM_011522134.1:c.5844G>T
|
XP_011520436.1:p.Met1948Ile
|
|
XM_005268276.5:c.11613G>T
|
XP_005268333.1:p.Met3871Ile
|
|
XM_006720726.3:c.11712G>T
|
XP_006720789.1:p.Met3904Ile
|
|
XM_006720727.3:c.11469G>T
|
XP_006720790.1:p.Met3823Ile
|
|
XM_017022695.1:c.11613G>T
|
XP_016878184.1:p.Met3871Ile
|
|
XM_017022696.1:c.11613G>T
|
XP_016878185.1:p.Met3871Ile
|
|
XM_017022697.1:c.4893G>T
|
XP_016878186.1:p.Met1631Ile
|
|
XM_017022698.1:c.4893G>T
|
XP_016878187.1:p.Met1631Ile
|
|
NM_004667.6:c.11727G>T
MANE Select
|
NP_004658.3:p.Met3909Ile
|
|