ENST00000261609.13:c.12014A>T
MANE Select
|
ENSP00000261609.8:p.Lys4005Met
|
|
ENST00000650509.1:c.3725A>T
|
ENSP00000496936.1:p.Lys1242Met
|
|
ENST00000261609.11:c.12014A>T
|
ENSP00000261609.7:p.Lys4005Met
|
|
NM_004667.5:c.12014A>T
|
NP_004658.3:p.Lys4005Met
|
|
XM_005268276.3:c.11900A>T
|
XP_005268333.1:p.Lys3967Met
|
|
XM_005268277.3:c.11900A>T
|
XP_005268334.1:p.Lys3967Met
|
|
XM_006720726.2:c.11999A>T
|
XP_006720789.1:p.Lys4000Met
|
|
XM_006720727.2:c.11756A>T
|
XP_006720790.1:p.Lys3919Met
|
|
XM_011522131.1:c.11531A>T
|
XP_011520433.1:p.Lys3844Met
|
|
XM_011522132.1:c.9530A>T
|
XP_011520434.1:p.Lys3177Met
|
|
XM_011522133.1:c.8759A>T
|
XP_011520435.1:p.Lys2920Met
|
|
XM_011522134.1:c.6131A>T
|
XP_011520436.1:p.Lys2044Met
|
|
XM_005268276.5:c.11900A>T
|
XP_005268333.1:p.Lys3967Met
|
|
XM_006720726.3:c.11999A>T
|
XP_006720789.1:p.Lys4000Met
|
|
XM_006720727.3:c.11756A>T
|
XP_006720790.1:p.Lys3919Met
|
|
XM_017022695.1:c.11900A>T
|
XP_016878184.1:p.Lys3967Met
|
|
XM_017022696.1:c.11900A>T
|
XP_016878185.1:p.Lys3967Met
|
|
XM_017022697.1:c.5180A>T
|
XP_016878186.1:p.Lys1727Met
|
|
XM_017022698.1:c.5180A>T
|
XP_016878187.1:p.Lys1727Met
|
|
NM_004667.6:c.12014A>T
MANE Select
|
NP_004658.3:p.Lys4005Met
|
|