ENST00000367324.8:c.852T>C
MANE Select
|
ENSP00000356293.4:p.Tyr284=
|
|
ENST00000263946.7:c.852T>C
|
ENSP00000263946.3:p.Tyr284=
|
|
ENST00000352845.3:c.852T>C
|
ENSP00000295597.3:p.Tyr284=
|
|
ENST00000367324.7:c.852T>C
|
ENSP00000356293.3:p.Tyr284=
|
|
ENST00000475988.1:n.194T>C
|
|
|
ENST00000622031.4:c.849T>C
|
ENSP00000482213.1:p.Tyr283=
|
|
NM_000299.3:c.852T>C
|
NP_000290.2:p.Tyr284=
|
|
NM_001005337.2:c.852T>C
|
NP_001005337.1:p.Tyr284=
|
|
NM_001005337.3:c.852T>C
MANE Select
|
NP_001005337.1:p.Tyr284=
|
|
NM_000299.4:c.852T>C
|
NP_000290.2:p.Tyr284=
|
|