ENST00000313468.10:c.385G>T
MANE Select
|
ENSP00000315774.5:p.Glu129Ter
|
|
ENST00000313468.9:c.385G>T
|
ENSP00000315774.5:p.Glu129Ter
|
|
ENST00000524810.5:c.317G>T
|
|
|
ENST00000525419.5:c.331G>T
|
ENSP00000433521.1:p.Glu111Ter
|
|
ENST00000526339.5:c.385G>T
|
ENSP00000436287.1:p.Glu129Ter
|
|
ENST00000526446.5:c.*440G>T
|
ENSP00000433645.1:n.*440G>T
|
|
ENST00000526542.1:n.336G>T
|
|
|
ENST00000528492.1:c.-54G>T
|
ENSP00000432848.1:n.-54G>T
|
|
ENST00000531282.1:n.237G>T
|
|
|
NM_002496.3:c.385G>T
|
NP_002487.1:p.Glu129Ter
|
|
XM_005274013.1:c.385G>T
|
XP_005274070.1:p.Glu129Ter
|
|
XM_005274014.1:c.385G>T
|
XP_005274071.1:p.Glu129Ter
|
|
XM_005274015.1:c.265G>T
|
XP_005274072.1:p.Glu89Ter
|
|
XM_011545053.1:c.385G>T
|
XP_011543355.1:p.Glu129Ter
|
|
NM_002496.4:c.385G>T
MANE Select
|
NP_002487.1:p.Glu129Ter
|
|