ENST00000426263.10:c.1145G>T
MANE Select
|
ENSP00000416293.2:p.Gly382Val
|
|
ENST00000674545.1:n.1762G>T
|
|
|
ENST00000674765.1:c.1030-881G>T
|
ENSP00000501811.1:n.1030-881G>T
|
|
ENST00000675112.1:n.1446G>T
|
|
|
ENST00000676254.1:n.1594G>T
|
|
|
ENST00000426263.7:c.1145G>T
|
ENSP00000416293.2:p.Gly382Val
|
|
ENST00000475162.3:c.416-760G>T
|
|
|
ENST00000630287.2:c.*460G>T
|
ENSP00000486694.1:n.*460G>T
|
|
NM_006516.2:c.1145G>T
|
NP_006507.2:p.Gly382Val
|
|
NM_006516.3:c.1145G>T
|
NP_006507.2:p.Gly382Val
|
|
NM_006516.4:c.1145G>T
MANE Select
|
NP_006507.2:p.Gly382Val
|
|