ENST00000313468.10:c.153G>T
MANE Select
|
ENSP00000315774.5:p.Val51=
|
|
ENST00000313468.9:c.153G>T
|
ENSP00000315774.5:p.Val51=
|
|
ENST00000432321.6:n.270G>T
|
|
|
ENST00000453471.6:c.153G>T
|
ENSP00000403972.2:p.Val51=
|
|
ENST00000525419.5:c.99G>T
|
ENSP00000433521.1:p.Val33=
|
|
ENST00000525628.1:c.153G>T
|
ENSP00000432968.1:p.Val51=
|
|
ENST00000526339.5:c.153G>T
|
ENSP00000436287.1:p.Val51=
|
|
ENST00000526446.5:c.*208G>T
|
ENSP00000433645.1:n.*208G>T
|
|
ENST00000528492.1:c.-67+2233G>T
|
ENSP00000432848.1:n.-67+2233G>T
|
|
ENST00000529645.1:c.331G>T
|
ENSP00000431293.1:n.331G>T
|
|
ENST00000531228.1:c.208G>T
|
ENSP00000433054.1:p.Asp70Tyr
|
|
ENST00000532399.1:n.760G>T
|
|
|
NM_002496.3:c.153G>T
|
NP_002487.1:p.Val51=
|
|
XM_005274013.1:c.153G>T
|
XP_005274070.1:p.Val51=
|
|
XM_005274014.1:c.153G>T
|
XP_005274071.1:p.Val51=
|
|
XM_005274015.1:c.33G>T
|
XP_005274072.1:p.Val11=
|
|
XM_011545053.1:c.153G>T
|
XP_011543355.1:p.Val51=
|
|
NM_002496.4:c.153G>T
MANE Select
|
NP_002487.1:p.Val51=
|
|