ENST00000336615.9:c.619G>A
MANE Select
|
ENSP00000337701.4:p.Val207Ile
|
|
ENST00000336615.8:c.619G>A
|
ENSP00000337701.4:p.Val207Ile
|
|
ENST00000525250.5:n.1225G>A
|
|
|
ENST00000531923.1:n.514G>A
|
|
|
ENST00000617551.1:c.-632G>A
|
ENSP00000481602.1:n.-632G>A
|
|
NM_020376.3:c.619G>A
|
NP_065109.1:p.Val207Ile
|
|
XM_006718265.2:c.619G>A
|
XP_006718328.1:p.Val207Ile
|
|
XM_006718266.2:c.619G>A
|
XP_006718329.1:p.Val207Ile
|
|
XM_006718265.3:c.619G>A
|
XP_006718328.1:p.Val207Ile
|
|
XM_006718266.3:c.619G>A
|
XP_006718329.1:p.Val207Ile
|
|
XM_017018028.1:c.619G>A
|
XP_016873517.1:p.Val207Ile
|
|
XM_024448618.1:c.619G>A
|
XP_024304386.1:p.Val207Ile
|
|
NM_020376.4:c.619G>A
MANE Select
|
NP_065109.1:p.Val207Ile
|
|