ENST00000449082.3:c.3217G>A
MANE Select
|
ENSP00000390600.2:p.Val1073Ile
|
|
ENST00000643924.1:c.3214G>A
|
ENSP00000495595.1:p.Val1072Ile
|
|
ENST00000655275.1:c.3241G>A
|
ENSP00000499510.1:p.Val1081Ile
|
|
ENST00000449082.2:c.3217G>A
|
ENSP00000390600.2:p.Val1073Ile
|
|
NM_001293306.2:c.3214G>A
|
NP_001280235.2:p.Val1072Ile
|
|
NM_001293307.2:c.2923G>A
|
NP_001280236.2:p.Val975Ile
|
|
NM_006514.3:c.3217G>A
|
NP_006505.3:p.Val1073Ile
|
|
XM_005265371.2:c.3226G>A
|
XP_005265428.1:p.Val1076Ile
|
|
XM_011533993.1:c.3223G>A
|
XP_011532295.1:p.Val1075Ile
|
|
XM_011533994.1:c.2932G>A
|
XP_011532296.1:p.Val978Ile
|
|
XM_005265371.3:c.3226G>A
|
XP_005265428.1:p.Val1076Ile
|
|
XM_011533993.2:c.3223G>A
|
XP_011532295.1:p.Val1075Ile
|
|
XM_011533994.2:c.2932G>A
|
XP_011532296.1:p.Val978Ile
|
|
NM_006514.4:c.3217G>A
MANE Select
|
NP_006505.4:p.Val1073Ile
|
|