ENST00000328300.11:c.4744G>A
MANE Select
|
ENSP00000331902.7:p.Val1582Ile
|
|
ENST00000361603.7:c.4726G>A
|
ENSP00000354505.2:p.Val1576Ile
|
|
ENST00000510690.2:n.1238G>A
|
|
|
ENST00000644079.1:n.1230G>A
|
|
|
ENST00000328300.10:c.4744G>A
|
ENSP00000331902.6:p.Val1582Ile
|
|
ENST00000361603.6:c.4726G>A
|
ENSP00000354505.2:p.Val1576Ile
|
|
ENST00000504541.1:c.142G>A
|
ENSP00000424845.1:p.Val48Ile
|
|
ENST00000515658.1:c.325-1453G>A
|
|
|
NM_000495.4:c.4726G>A
|
NP_000486.1:p.Val1576Ile
|
|
NM_033380.2:c.4744G>A
|
NP_203699.1:p.Val1582Ile
|
|
XM_005262070.2:c.4735G>A
|
XP_005262127.1:p.Val1579Ile
|
|
XM_006724616.2:c.4744G>A
|
XP_006724679.1:p.Val1582Ile
|
|
XM_011530849.1:c.4420G>A
|
XP_011529151.1:p.Val1474Ile
|
|
XM_011530851.1:c.2317G>A
|
XP_011529153.1:p.Val773Ile
|
|
XM_011530849.2:c.4759G>A
|
XP_011529151.2:p.Val1587Ile
|
|
XM_017029259.2:c.4750G>A
|
XP_016884748.1:p.Val1584Ile
|
|
XM_017029260.1:c.4741G>A
|
XP_016884749.1:p.Val1581Ile
|
|
XM_017029263.2:c.3079G>A
|
XP_016884752.1:p.Val1027Ile
|
|
NM_000495.5:c.4726G>A
|
NP_000486.1:p.Val1576Ile
|
|
NM_033380.3:c.4744G>A
MANE Select
|
NP_203699.1:p.Val1582Ile
|
|