ENST00000262367.10:c.2053T>C
MANE Select
|
ENSP00000262367.5:p.Leu685=
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|
ENST00000262367.9:c.2053T>C
|
ENSP00000262367.5:p.Leu685=
|
|
ENST00000382070.7:c.1939T>C
|
ENSP00000371502.3:p.Leu647=
|
|
ENST00000570939.2:c.658T>C
|
ENSP00000461002.2:p.Leu220=
|
|
ENST00000571826.5:c.102T>C
|
|
|
ENST00000572134.1:c.366T>C
|
|
|
ENST00000634839.1:n.215T>C
|
|
|
NM_001079846.1:c.1939T>C
|
NP_001073315.1:p.Leu647=
|
|
NM_004380.2:c.2053T>C
|
NP_004371.2:p.Leu685=
|
|
XM_005255124.3:c.2053T>C
|
XP_005255181.1:p.Leu685=
|
|
XM_005255125.3:c.2053T>C
|
XP_005255182.1:p.Leu685=
|
|
XM_006720848.2:c.2053T>C
|
XP_006720911.1:p.Leu685=
|
|
XM_011522380.1:c.1999T>C
|
XP_011520682.1:p.Leu667=
|
|
XM_011522381.1:c.1300T>C
|
XP_011520683.1:p.Leu434=
|
|
XM_011522382.1:c.2053T>C
|
XP_011520684.1:p.Leu685=
|
|
XM_005255124.4:c.2053T>C
|
XP_005255181.1:p.Leu685=
|
|
XM_005255125.4:c.2053T>C
|
XP_005255182.1:p.Leu685=
|
|
XM_006720848.3:c.2053T>C
|
XP_006720911.1:p.Leu685=
|
|
XM_011522381.2:c.1300T>C
|
XP_011520683.1:p.Leu434=
|
|
XM_011522382.3:c.2053T>C
|
XP_011520684.1:p.Leu685=
|
|
XM_017022944.1:c.2053T>C
|
XP_016878433.1:p.Leu685=
|
|
NM_004380.3:c.2053T>C
MANE Select
|
NP_004371.2:p.Leu685=
|
|