ENST00000299506.3:c.253G>A
MANE Select
|
ENSP00000299506.3:p.Val85Ile
|
|
ENST00000299506.2:c.253G>A
|
ENSP00000299506.2:p.Val85Ile
|
|
ENST00000305253.8:c.418G>A
|
ENSP00000305426.4:p.Val140Ile
|
|
ENST00000534099.5:c.271G>A
|
ENSP00000434400.1:p.Val91Ile
|
|
NM_003320.4:c.418G>A
|
NP_003311.2:p.Val140Ile
|
|
NM_177972.2:c.253G>A
|
NP_813977.1:p.Val85Ile
|
|
XM_005253109.2:c.379G>A
|
XP_005253166.1:p.Val127Ile
|
|
XM_011520344.1:c.289G>A
|
XP_011518646.1:p.Val97Ile
|
|
XM_005253109.3:c.379G>A
|
XP_005253166.1:p.Val127Ile
|
|
XM_011520344.2:c.289G>A
|
XP_011518646.1:p.Val97Ile
|
|
NM_177972.3:c.253G>A
MANE Select
|
NP_813977.1:p.Val85Ile
|
|
NM_003320.5:c.418G>A
|
NP_003311.2:p.Val140Ile
|
|