|
NM_000069.3:c.4504A>G
MANE Select
|
NP_000060.2:p.Ser1502Gly
|
|
ENST00000362061.4:c.4504A>G
MANE Select
|
ENSP00000355192.3:p.Ser1502Gly
|
|
NM_000069.2:c.4504A>G
|
NP_000060.2:p.Ser1502Gly
|
|
ENST00000362061.3:c.4504A>G
|
ENSP00000355192.3:p.Ser1502Gly
|
|
ENST00000367338.7:c.4447A>G
|
ENSP00000356307.3:p.Ser1483Gly
|
|
ENST00000679417.1:c.*3667A>G
|
ENSP00000506706.1:n.*3667A>G
|
|
ENST00000680051.1:n.1630A>G
|
|
|
ENST00000680059.1:c.*2022A>G
|
ENSP00000504944.1:n.*2022A>G
|
|
ENST00000681078.1:c.*279A>G
|
ENSP00000506645.1:n.*279A>G
|
|
ENST00000681190.1:c.*686A>G
|
ENSP00000506428.1:n.*686A>G
|
|
ENST00000681874.1:c.4444A>G
|
ENSP00000505162.1:p.Ser1482Gly
|
|
XM_005245478.2:c.4447A>G
|
XP_005245535.1:p.Ser1483Gly
|
|
XM_005245478.3:c.4447A>G
|
XP_005245535.1:p.Ser1483Gly
|