ENST00000449082.3:c.4849G>A
MANE Select
|
ENSP00000390600.2:p.Val1617Ile
|
|
ENST00000643924.1:c.4846G>A
|
ENSP00000495595.1:p.Val1616Ile
|
|
ENST00000655275.1:c.4873G>A
|
ENSP00000499510.1:p.Val1625Ile
|
|
ENST00000449082.2:c.4849G>A
|
ENSP00000390600.2:p.Val1617Ile
|
|
NM_001293306.2:c.4846G>A
|
NP_001280235.2:p.Val1616Ile
|
|
NM_001293307.2:c.4555G>A
|
NP_001280236.2:p.Val1519Ile
|
|
NM_006514.3:c.4849G>A
|
NP_006505.3:p.Val1617Ile
|
|
XM_005265371.2:c.4858G>A
|
XP_005265428.1:p.Val1620Ile
|
|
XM_011533993.1:c.4855G>A
|
XP_011532295.1:p.Val1619Ile
|
|
XM_011533994.1:c.4564G>A
|
XP_011532296.1:p.Val1522Ile
|
|
XM_005265371.3:c.4858G>A
|
XP_005265428.1:p.Val1620Ile
|
|
XM_011533993.2:c.4855G>A
|
XP_011532295.1:p.Val1619Ile
|
|
XM_011533994.2:c.4564G>A
|
XP_011532296.1:p.Val1522Ile
|
|
NM_006514.4:c.4849G>A
MANE Select
|
NP_006505.4:p.Val1617Ile
|
|