ENST00000328300.11:c.4972G>A
MANE Select
|
ENSP00000331902.7:p.Val1658Ile
|
|
ENST00000361603.7:c.4954G>A
|
ENSP00000354505.2:p.Val1652Ile
|
|
ENST00000510690.2:n.1466G>A
|
|
|
ENST00000644079.1:n.1803G>A
|
|
|
ENST00000328300.10:c.4972G>A
|
ENSP00000331902.6:p.Val1658Ile
|
|
ENST00000361603.6:c.4954G>A
|
ENSP00000354505.2:p.Val1652Ile
|
|
ENST00000504541.1:c.219+496G>A
|
ENSP00000424845.1:n.219+496G>A
|
|
ENST00000515658.1:c.325-880G>A
|
|
|
NM_000495.4:c.4954G>A
|
NP_000486.1:p.Val1652Ile
|
|
NM_033380.2:c.4972G>A
|
NP_203699.1:p.Val1658Ile
|
|
XM_005262070.2:c.4963G>A
|
XP_005262127.1:p.Val1655Ile
|
|
XM_006724616.2:c.4972G>A
|
XP_006724679.1:p.Val1658Ile
|
|
XM_011530849.1:c.4648G>A
|
XP_011529151.1:p.Val1550Ile
|
|
XM_011530851.1:c.2545G>A
|
XP_011529153.1:p.Val849Ile
|
|
XM_011530849.2:c.4987G>A
|
XP_011529151.2:p.Val1663Ile
|
|
XM_017029259.2:c.4978G>A
|
XP_016884748.1:p.Val1660Ile
|
|
XM_017029260.1:c.4969G>A
|
XP_016884749.1:p.Val1657Ile
|
|
XM_017029263.2:c.3307G>A
|
XP_016884752.1:p.Val1103Ile
|
|
NM_000495.5:c.4954G>A
|
NP_000486.1:p.Val1652Ile
|
|
NM_033380.3:c.4972G>A
MANE Select
|
NP_203699.1:p.Val1658Ile
|
|