ENST00000313468.10:c.387G>A
MANE Select
|
ENSP00000315774.5:p.Glu129=
|
|
ENST00000313468.9:c.387G>A
|
ENSP00000315774.5:p.Glu129=
|
|
ENST00000524810.5:c.319G>A
|
|
|
ENST00000525419.5:c.333G>A
|
ENSP00000433521.1:p.Glu111=
|
|
ENST00000526339.5:c.387G>A
|
ENSP00000436287.1:p.Glu129=
|
|
ENST00000526446.5:c.*442G>A
|
ENSP00000433645.1:n.*442G>A
|
|
ENST00000526542.1:n.338G>A
|
|
|
ENST00000528492.1:c.-52G>A
|
ENSP00000432848.1:n.-52G>A
|
|
ENST00000531282.1:n.239G>A
|
|
|
NM_002496.3:c.387G>A
|
NP_002487.1:p.Glu129=
|
|
XM_005274013.1:c.387G>A
|
XP_005274070.1:p.Glu129=
|
|
XM_005274014.1:c.387G>A
|
XP_005274071.1:p.Glu129=
|
|
XM_005274015.1:c.267G>A
|
XP_005274072.1:p.Glu89=
|
|
XM_011545053.1:c.387G>A
|
XP_011543355.1:p.Glu129=
|
|
NM_002496.4:c.387G>A
MANE Select
|
NP_002487.1:p.Glu129=
|
|