ENST00000313468.10:c.162G>T
MANE Select
|
ENSP00000315774.5:p.Arg54=
|
|
ENST00000313468.9:c.162G>T
|
ENSP00000315774.5:p.Arg54=
|
|
ENST00000432321.6:n.279G>T
|
|
|
ENST00000453471.6:c.162G>T
|
ENSP00000403972.2:p.Arg54=
|
|
ENST00000525419.5:c.108G>T
|
ENSP00000433521.1:p.Arg36=
|
|
ENST00000525628.1:c.162G>T
|
ENSP00000432968.1:p.Arg54=
|
|
ENST00000526339.5:c.162G>T
|
ENSP00000436287.1:p.Arg54=
|
|
ENST00000526446.5:c.*217G>T
|
ENSP00000433645.1:n.*217G>T
|
|
ENST00000528492.1:c.-67+2242G>T
|
ENSP00000432848.1:n.-67+2242G>T
|
|
ENST00000529645.1:c.340G>T
|
ENSP00000431293.1:n.340G>T
|
|
ENST00000531228.1:c.*4G>T
|
ENSP00000433054.1:n.*4G>T
|
|
ENST00000532399.1:n.769G>T
|
|
|
NM_002496.3:c.162G>T
|
NP_002487.1:p.Arg54=
|
|
XM_005274013.1:c.162G>T
|
XP_005274070.1:p.Arg54=
|
|
XM_005274014.1:c.162G>T
|
XP_005274071.1:p.Arg54=
|
|
XM_005274015.1:c.42G>T
|
XP_005274072.1:p.Arg14=
|
|
XM_011545053.1:c.162G>T
|
XP_011543355.1:p.Arg54=
|
|
NM_002496.4:c.162G>T
MANE Select
|
NP_002487.1:p.Arg54=
|
|