ENST00000261609.13:c.11715T>A
MANE Select
|
ENSP00000261609.8:p.Ile3905=
|
|
ENST00000650509.1:c.3426T>A
|
ENSP00000496936.1:p.Ile1142=
|
|
ENST00000261609.11:c.11715T>A
|
ENSP00000261609.7:p.Ile3905=
|
|
ENST00000564519.1:n.230T>A
|
|
|
NM_004667.5:c.11715T>A
|
NP_004658.3:p.Ile3905=
|
|
XM_005268276.3:c.11601T>A
|
XP_005268333.1:p.Ile3867=
|
|
XM_005268277.3:c.11601T>A
|
XP_005268334.1:p.Ile3867=
|
|
XM_006720726.2:c.11700T>A
|
XP_006720789.1:p.Ile3900=
|
|
XM_006720727.2:c.11457T>A
|
XP_006720790.1:p.Ile3819=
|
|
XM_011522131.1:c.11232T>A
|
XP_011520433.1:p.Ile3744=
|
|
XM_011522132.1:c.9231T>A
|
XP_011520434.1:p.Ile3077=
|
|
XM_011522133.1:c.8460T>A
|
XP_011520435.1:p.Ile2820=
|
|
XM_011522134.1:c.5832T>A
|
XP_011520436.1:p.Ile1944=
|
|
XM_005268276.5:c.11601T>A
|
XP_005268333.1:p.Ile3867=
|
|
XM_006720726.3:c.11700T>A
|
XP_006720789.1:p.Ile3900=
|
|
XM_006720727.3:c.11457T>A
|
XP_006720790.1:p.Ile3819=
|
|
XM_017022695.1:c.11601T>A
|
XP_016878184.1:p.Ile3867=
|
|
XM_017022696.1:c.11601T>A
|
XP_016878185.1:p.Ile3867=
|
|
XM_017022697.1:c.4881T>A
|
XP_016878186.1:p.Ile1627=
|
|
XM_017022698.1:c.4881T>A
|
XP_016878187.1:p.Ile1627=
|
|
NM_004667.6:c.11715T>A
MANE Select
|
NP_004658.3:p.Ile3905=
|
|