ENST00000335606.11:c.671G>T
(AMACR)
MANE Select
|
ENSP00000334424.6:p.Arg224Met
|
|
ENST00000335606.10:c.671G>T
(AMACR)
|
ENSP00000334424.6:p.Arg224Met
|
|
ENST00000382068.3:c.510G>T
(AMACR)
|
ENSP00000477108.1:p.Gln170His
|
|
ENST00000382072.6:c.510G>T
(AMACR)
|
ENSP00000371504.2:p.Gln170His
|
|
ENST00000382079.3:c.*97G>T
(C1QTNF3-AMACR)
|
ENSP00000371511.3:n.*97G>T
|
|
ENST00000382085.7:c.671G>T
(AMACR)
|
ENSP00000371517.3:p.Arg224Met
|
|
ENST00000426255.6:c.671G>T
(AMACR)
|
ENSP00000476965.1:p.Arg224Met
|
|
ENST00000502637.5:c.626G>T
(AMACR)
|
ENSP00000424351.1:p.Arg209Met
|
|
ENST00000506639.5:c.510G>T
(AMACR)
|
ENSP00000427227.1:p.Gln170His
|
|
ENST00000512079.5:c.671G>T
(AMACR)
|
ENSP00000477411.1:p.Arg224Met
|
|
ENST00000514195.1:n.522G>T
(AMACR)
|
|
|
NM_001167595.1:c.671G>T
(AMACR)
|
NP_001161067.1:p.Arg224Met
|
|
NM_014324.5:c.671G>T
(AMACR)
|
NP_055139.4:p.Arg224Met
|
|
NM_203382.2:c.510G>T
(AMACR)
|
NP_976316.1:p.Gln170His
|
|
NR_037951.1:n.1027G>T
(C1QTNF3-AMACR)
|
|
|
NM_014324.6:c.671G>T
(AMACR)
MANE Select
|
NP_055139.4:p.Arg224Met
|
|
NM_001167595.2:c.671G>T
(AMACR)
|
NP_001161067.1:p.Arg224Met
|
|
NM_203382.3:c.510G>T
(AMACR)
|
NP_976316.1:p.Gln170His
|
|