ENST00000456935.7:c.357G>A
MANE Select
|
ENSP00000395473.2:p.Val119=
|
|
ENST00000221363.8:c.357G>A
|
ENSP00000221363.4:p.Val119=
|
|
ENST00000456935.6:c.357G>A
|
ENSP00000395473.2:p.Val119=
|
|
ENST00000466794.5:n.339G>A
|
|
|
ENST00000486847.2:c.254G>A
|
ENSP00000470174.1:p.Trp85Ter
|
|
ENST00000596512.5:n.295G>A
|
|
|
ENST00000597961.1:c.348G>A
|
ENSP00000472710.1:p.Val116=
|
|
ENST00000598876.1:c.384G>A
|
ENSP00000470533.1:p.Val128=
|
|
ENST00000600281.1:n.398G>A
|
|
|
NM_000528.3:c.357G>A
|
NP_000519.2:p.Val119=
|
|
NM_001173498.1:c.357G>A
|
NP_001166969.1:p.Val119=
|
|
XM_005259913.1:c.357G>A
|
XP_005259970.1:p.Val119=
|
|
XM_005259913.2:c.357G>A
|
XP_005259970.1:p.Val119=
|
|
XM_024451518.1:c.-662G>A
|
XP_024307286.1:n.-662G>A
|
|
NM_000528.4:c.357G>A
MANE Select
|
NP_000519.2:p.Val119=
|
|
NM_001173498.2:c.357G>A
|
NP_001166969.1:p.Val119=
|
|