ENST00000328300.11:c.4840G>T
MANE Select
|
ENSP00000331902.7:p.Glu1614Ter
|
|
ENST00000361603.7:c.4822G>T
|
ENSP00000354505.2:p.Glu1608Ter
|
|
ENST00000510690.2:n.1334G>T
|
|
|
ENST00000644079.1:n.1671G>T
|
|
|
ENST00000328300.10:c.4840G>T
|
ENSP00000331902.6:p.Glu1614Ter
|
|
ENST00000361603.6:c.4822G>T
|
ENSP00000354505.2:p.Glu1608Ter
|
|
ENST00000504541.1:c.219+364G>T
|
ENSP00000424845.1:n.219+364G>T
|
|
ENST00000515658.1:c.325-1012G>T
|
|
|
NM_000495.4:c.4822G>T
|
NP_000486.1:p.Glu1608Ter
|
|
NM_033380.2:c.4840G>T
|
NP_203699.1:p.Glu1614Ter
|
|
XM_005262070.2:c.4831G>T
|
XP_005262127.1:p.Glu1611Ter
|
|
XM_006724616.2:c.4840G>T
|
XP_006724679.1:p.Glu1614Ter
|
|
XM_011530849.1:c.4516G>T
|
XP_011529151.1:p.Glu1506Ter
|
|
XM_011530851.1:c.2413G>T
|
XP_011529153.1:p.Glu805Ter
|
|
XM_011530849.2:c.4855G>T
|
XP_011529151.2:p.Glu1619Ter
|
|
XM_017029259.2:c.4846G>T
|
XP_016884748.1:p.Glu1616Ter
|
|
XM_017029260.1:c.4837G>T
|
XP_016884749.1:p.Glu1613Ter
|
|
XM_017029263.2:c.3175G>T
|
XP_016884752.1:p.Glu1059Ter
|
|
NM_000495.5:c.4822G>T
|
NP_000486.1:p.Glu1608Ter
|
|
NM_033380.3:c.4840G>T
MANE Select
|
NP_203699.1:p.Glu1614Ter
|
|