ENST00000328300.11:c.5061C>A
MANE Select
|
ENSP00000331902.7:p.Cys1687Ter
|
|
ENST00000361603.7:c.5043C>A
|
ENSP00000354505.2:p.Cys1681Ter
|
|
ENST00000510690.2:n.1555C>A
|
|
|
ENST00000644079.1:n.2749C>A
|
|
|
ENST00000328300.10:c.5061C>A
|
ENSP00000331902.6:p.Cys1687Ter
|
|
ENST00000361603.6:c.5043C>A
|
ENSP00000354505.2:p.Cys1681Ter
|
|
ENST00000504541.1:c.286C>A
|
ENSP00000424845.1:n.286C>A
|
|
ENST00000515658.1:c.391C>A
|
|
|
NM_000495.4:c.5043C>A
|
NP_000486.1:p.Cys1681Ter
|
|
NM_033380.2:c.5061C>A
|
NP_203699.1:p.Cys1687Ter
|
|
XM_005262070.2:c.5052C>A
|
XP_005262127.1:p.Cys1684Ter
|
|
XM_006724616.2:c.5061C>A
|
XP_006724679.1:p.Cys1687Ter
|
|
XM_011530849.1:c.4737C>A
|
XP_011529151.1:p.Cys1579Ter
|
|
XM_011530851.1:c.2634C>A
|
XP_011529153.1:p.Cys878Ter
|
|
XM_011530849.2:c.5076C>A
|
XP_011529151.2:p.Cys1692Ter
|
|
XM_017029259.2:c.5067C>A
|
XP_016884748.1:p.Cys1689Ter
|
|
XM_017029260.1:c.5058C>A
|
XP_016884749.1:p.Cys1686Ter
|
|
XM_017029263.2:c.3396C>A
|
XP_016884752.1:p.Cys1132Ter
|
|
NM_000495.5:c.5043C>A
|
NP_000486.1:p.Cys1681Ter
|
|
NM_033380.3:c.5061C>A
MANE Select
|
NP_203699.1:p.Cys1687Ter
|
|