ENST00000371486.4:c.1666T>C
MANE Select
|
ENSP00000360541.3:p.Leu556=
|
|
ENST00000635862.1:c.1633T>C
|
ENSP00000490867.1:p.Leu545=
|
|
ENST00000635888.1:c.*1652T>C
|
ENSP00000490042.1:n.*1652T>C
|
|
ENST00000636239.1:c.*1313T>C
|
ENSP00000490066.1:n.*1313T>C
|
|
ENST00000636867.1:c.1597T>C
|
ENSP00000489631.1:p.Leu533=
|
|
ENST00000636891.1:c.1716T>C
|
ENSP00000490399.1:p.Thr572=
|
|
ENST00000636935.1:c.361T>C
|
ENSP00000489757.1:p.Leu121=
|
|
ENST00000637252.1:c.1702T>C
|
ENSP00000490492.1:p.Leu568=
|
|
ENST00000638135.1:c.*1313T>C
|
ENSP00000489756.1:n.*1313T>C
|
|
ENST00000371486.3:c.1666T>C
|
ENSP00000360541.3:p.Leu556=
|
|
NM_000098.2:c.1666T>C
|
NP_000089.1:p.Leu556=
|
|
XM_005270484.1:c.1597T>C
|
XP_005270541.1:p.Leu533=
|
|
NM_001330589.1:c.1597T>C
|
NP_001317518.1:p.Leu533=
|
|
NM_000098.3:c.1666T>C
MANE Select
|
NP_000089.1:p.Leu556=
|
|
NM_001330589.2:c.1597T>C
|
NP_001317518.1:p.Leu533=
|
|