ENST00000376020.9:c.4066G>A
MANE Select
|
ENSP00000365188.2:p.Val1356Ile
|
|
ENST00000376020.8:c.4066G>A
|
ENSP00000365188.2:p.Val1356Ile
|
|
ENST00000289292.11:c.4066G>A
|
ENSP00000289292.7:p.Val1356Ile
|
|
ENST00000376020.6:c.4066G>A
|
ENSP00000365188.2:p.Val1356Ile
|
|
ENST00000460112.3:c.3718G>A
|
ENSP00000421450.1:p.Val1240Ile
|
|
NM_020717.3:c.4066G>A
|
NP_065768.2:p.Val1356Ile
|
|
NR_027121.1:n.4092G>A
|
|
|
XM_006724590.2:c.3718G>A
|
XP_006724653.1:p.Val1240Ile
|
|
XM_006724591.2:c.3592G>A
|
XP_006724654.1:p.Val1198Ile
|
|
XM_011530800.1:c.3931G>A
|
XP_011529102.1:p.Val1311Ile
|
|
XM_011530801.1:c.4067G>A
|
XP_011529103.1:p.Arg1356His
|
|
XR_938367.1:n.4184G>A
|
|
|
XR_938368.1:n.4184G>A
|
|
|
XM_017029682.2:c.4180G>A
|
XP_016885171.1:p.Val1394Ile
|
|
XM_017029683.1:c.4045G>A
|
XP_016885172.1:p.Val1349Ile
|
|
XM_017029684.1:c.3832G>A
|
XP_016885173.1:p.Val1278Ile
|
|
XM_017029685.2:c.4181G>A
|
XP_016885174.1:p.Arg1394His
|
|
XM_017029686.1:c.3706G>A
|
XP_016885175.1:p.Val1236Ile
|
|
XR_001755716.2:n.4311G>A
|
|
|
XR_001755717.2:n.4311G>A
|
|
|
XR_001755718.2:n.4311G>A
|
|
|
NM_020717.5:c.4066G>A
MANE Select
|
NP_065768.2:p.Val1356Ile
|
|
NR_027121.3:n.4242G>A
|
|
|
NR_172068.1:n.4107G>A
|
|
|
NR_172069.1:n.4162G>A
|
|
|
NR_172070.1:n.4027G>A
|
|
|