ENST00000426263.10:c.1074G>C
MANE Select
|
ENSP00000416293.2:p.Leu358=
|
|
ENST00000674545.1:n.568G>C
|
|
|
ENST00000674765.1:c.1029+45G>C
|
ENSP00000501811.1:n.1029+45G>C
|
|
ENST00000675112.1:n.1375G>C
|
|
|
ENST00000676254.1:n.1523G>C
|
|
|
ENST00000426263.7:c.1074G>C
|
ENSP00000416293.2:p.Leu358=
|
|
ENST00000475162.3:c.415+1694G>C
|
|
|
ENST00000630287.2:c.*389G>C
|
ENSP00000486694.1:n.*389G>C
|
|
NM_006516.2:c.1074G>C
|
NP_006507.2:p.Leu358=
|
|
NM_006516.3:c.1074G>C
|
NP_006507.2:p.Leu358=
|
|
NM_006516.4:c.1074G>C
MANE Select
|
NP_006507.2:p.Leu358=
|
|