ENST00000261609.13:c.11706T>A
MANE Select
|
ENSP00000261609.8:p.Ala3902=
|
|
ENST00000650509.1:c.3417T>A
|
ENSP00000496936.1:p.Ala1139=
|
|
ENST00000261609.11:c.11706T>A
|
ENSP00000261609.7:p.Ala3902=
|
|
ENST00000564519.1:n.221T>A
|
|
|
NM_004667.5:c.11706T>A
|
NP_004658.3:p.Ala3902=
|
|
XM_005268276.3:c.11592T>A
|
XP_005268333.1:p.Ala3864=
|
|
XM_005268277.3:c.11592T>A
|
XP_005268334.1:p.Ala3864=
|
|
XM_006720726.2:c.11691T>A
|
XP_006720789.1:p.Ala3897=
|
|
XM_006720727.2:c.11448T>A
|
XP_006720790.1:p.Ala3816=
|
|
XM_011522131.1:c.11223T>A
|
XP_011520433.1:p.Ala3741=
|
|
XM_011522132.1:c.9222T>A
|
XP_011520434.1:p.Ala3074=
|
|
XM_011522133.1:c.8451T>A
|
XP_011520435.1:p.Ala2817=
|
|
XM_011522134.1:c.5823T>A
|
XP_011520436.1:p.Ala1941=
|
|
XM_005268276.5:c.11592T>A
|
XP_005268333.1:p.Ala3864=
|
|
XM_006720726.3:c.11691T>A
|
XP_006720789.1:p.Ala3897=
|
|
XM_006720727.3:c.11448T>A
|
XP_006720790.1:p.Ala3816=
|
|
XM_017022695.1:c.11592T>A
|
XP_016878184.1:p.Ala3864=
|
|
XM_017022696.1:c.11592T>A
|
XP_016878185.1:p.Ala3864=
|
|
XM_017022697.1:c.4872T>A
|
XP_016878186.1:p.Ala1624=
|
|
XM_017022698.1:c.4872T>A
|
XP_016878187.1:p.Ala1624=
|
|
NM_004667.6:c.11706T>A
MANE Select
|
NP_004658.3:p.Ala3902=
|
|