ENST00000261978.9:c.5365G>A
MANE Select
|
ENSP00000261978.4:p.Val1789Ile
|
|
ENST00000261978.8:c.5365G>A
|
ENSP00000261978.4:p.Val1789Ile
|
|
ENST00000553939.5:c.*144G>A
|
ENSP00000452110.1:n.*144G>A
|
|
ENST00000554861.1:n.583G>A
|
|
|
ENST00000556690.5:c.5233G>A
|
ENSP00000451477.1:p.Val1745Ile
|
|
NM_000428.2:c.5365G>A
|
NP_000419.1:p.Val1789Ile
|
|
XM_011536765.1:c.4984G>A
|
XP_011535067.1:p.Val1662Ile
|
|
XM_011536766.1:c.4906G>A
|
XP_011535068.1:p.Val1636Ile
|
|
XM_011536767.1:c.4882G>A
|
XP_011535069.1:p.Val1628Ile
|
|
XM_011536765.2:c.4984G>A
|
XP_011535067.1:p.Val1662Ile
|
|
NM_000428.3:c.5365G>A
MANE Select
|
NP_000419.1:p.Val1789Ile
|
|