ENST00000426263.10:c.1143G>C
MANE Select
|
ENSP00000416293.2:p.Val381=
|
|
ENST00000674545.1:n.1760G>C
|
|
|
ENST00000674765.1:c.1030-883G>C
|
ENSP00000501811.1:n.1030-883G>C
|
|
ENST00000675112.1:n.1444G>C
|
|
|
ENST00000676254.1:n.1592G>C
|
|
|
ENST00000426263.7:c.1143G>C
|
ENSP00000416293.2:p.Val381=
|
|
ENST00000475162.3:c.416-762G>C
|
|
|
ENST00000630287.2:c.*458G>C
|
ENSP00000486694.1:n.*458G>C
|
|
NM_006516.2:c.1143G>C
|
NP_006507.2:p.Val381=
|
|
NM_006516.3:c.1143G>C
|
NP_006507.2:p.Val381=
|
|
NM_006516.4:c.1143G>C
MANE Select
|
NP_006507.2:p.Val381=
|
|