ENST00000553106.6:c.993T>C
MANE Select
|
ENSP00000448059.1:p.Phe331=
|
|
ENST00000307000.7:c.978T>C
|
ENSP00000303500.2:p.Phe326=
|
|
ENST00000549247.6:n.752T>C
|
|
|
ENST00000551114.2:n.655T>C
|
|
|
ENST00000553106.5:c.993T>C
|
ENSP00000448059.1:p.Phe331=
|
|
ENST00000635477.1:c.97T>C
|
|
|
ENST00000635528.1:n.508T>C
|
|
|
NM_000277.1:c.993T>C
|
NP_000268.1:p.Phe331=
|
|
XM_011538422.1:c.936T>C
|
XP_011536724.1:p.Phe312=
|
|
NM_000277.2:c.993T>C
|
NP_000268.1:p.Phe331=
|
|
NM_001354304.1:c.993T>C
|
NP_001341233.1:p.Phe331=
|
|
NM_000277.3:c.993T>C
MANE Select
|
NP_000268.1:p.Phe331=
|
|
NM_001354304.2:c.993T>C
|
NP_001341233.1:p.Phe331=
|
|