ENST00000313468.10:c.356C>T
MANE Select
|
ENSP00000315774.5:p.Ala119Val
|
|
ENST00000313468.9:c.356C>T
|
ENSP00000315774.5:p.Ala119Val
|
|
ENST00000432321.6:n.473C>T
|
|
|
ENST00000453471.6:c.356C>T
|
ENSP00000403972.2:p.Ala119Val
|
|
ENST00000524810.5:c.127C>T
|
|
|
ENST00000525419.5:c.302C>T
|
ENSP00000433521.1:p.Ala101Val
|
|
ENST00000526339.5:c.356C>T
|
ENSP00000436287.1:p.Ala119Val
|
|
ENST00000526446.5:c.*411C>T
|
ENSP00000433645.1:n.*411C>T
|
|
ENST00000528492.1:c.-67+2534C>T
|
ENSP00000432848.1:n.-67+2534C>T
|
|
ENST00000529645.1:c.534C>T
|
ENSP00000431293.1:n.534C>T
|
|
ENST00000532399.1:n.1061C>T
|
|
|
NM_002496.3:c.356C>T
|
NP_002487.1:p.Ala119Val
|
|
XM_005274013.1:c.356C>T
|
XP_005274070.1:p.Ala119Val
|
|
XM_005274014.1:c.356C>T
|
XP_005274071.1:p.Ala119Val
|
|
XM_005274015.1:c.236C>T
|
XP_005274072.1:p.Ala79Val
|
|
XM_011545053.1:c.356C>T
|
XP_011543355.1:p.Ala119Val
|
|
NM_002496.4:c.356C>T
MANE Select
|
NP_002487.1:p.Ala119Val
|
|