ENST00000496887.7:c.1179C>G
|
ENSP00000434560.2:p.Ala393=
|
|
ENST00000646564.2:c.996C>G
|
ENSP00000495806.2:p.Ala332=
|
|
ENST00000155840.12:c.1536C>G
MANE Select
|
ENSP00000155840.2:p.Ala512=
|
|
ENST00000335475.6:c.1155C>G
|
ENSP00000334497.5:p.Ala385=
|
|
ENST00000646564.1:c.642C>G
|
ENSP00000495806.1:p.Ala214=
|
|
ENST00000155840.9:c.1536C>G
|
ENSP00000155840.2:p.Ala512=
|
|
ENST00000335475.5:c.1155C>G
|
ENSP00000334497.5:p.Ala385=
|
|
NM_000218.2:c.1536C>G , LRG_287t1:c.1536C>G
|
NP_000209.2:p.Ala512=
|
|
NM_181798.1:c.1155C>G , LRG_287t2:c.1155C>G
|
NP_861463.1:p.Ala385=
|
|
NM_000218.3:c.1536C>G
MANE Select
|
NP_000209.2:p.Ala512=
|
|