ENST00000261609.13:c.11802G>T
MANE Select
|
ENSP00000261609.8:p.Val3934=
|
|
ENST00000650509.1:c.3513G>T
|
ENSP00000496936.1:p.Val1171=
|
|
ENST00000261609.11:c.11802G>T
|
ENSP00000261609.7:p.Val3934=
|
|
ENST00000564519.1:n.317G>T
|
|
|
NM_004667.5:c.11802G>T
|
NP_004658.3:p.Val3934=
|
|
XM_005268276.3:c.11688G>T
|
XP_005268333.1:p.Val3896=
|
|
XM_005268277.3:c.11688G>T
|
XP_005268334.1:p.Val3896=
|
|
XM_006720726.2:c.11787G>T
|
XP_006720789.1:p.Val3929=
|
|
XM_006720727.2:c.11544G>T
|
XP_006720790.1:p.Val3848=
|
|
XM_011522131.1:c.11319G>T
|
XP_011520433.1:p.Val3773=
|
|
XM_011522132.1:c.9318G>T
|
XP_011520434.1:p.Val3106=
|
|
XM_011522133.1:c.8547G>T
|
XP_011520435.1:p.Val2849=
|
|
XM_011522134.1:c.5919G>T
|
XP_011520436.1:p.Val1973=
|
|
XM_005268276.5:c.11688G>T
|
XP_005268333.1:p.Val3896=
|
|
XM_006720726.3:c.11787G>T
|
XP_006720789.1:p.Val3929=
|
|
XM_006720727.3:c.11544G>T
|
XP_006720790.1:p.Val3848=
|
|
XM_017022695.1:c.11688G>T
|
XP_016878184.1:p.Val3896=
|
|
XM_017022696.1:c.11688G>T
|
XP_016878185.1:p.Val3896=
|
|
XM_017022697.1:c.4968G>T
|
XP_016878186.1:p.Val1656=
|
|
XM_017022698.1:c.4968G>T
|
XP_016878187.1:p.Val1656=
|
|
NM_004667.6:c.11802G>T
MANE Select
|
NP_004658.3:p.Val3934=
|
|