ENST00000496887.7:c.187G=
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ENSP00000434560.2:p.Ala63=
|
|
ENST00000646564.2:c.448G=
|
ENSP00000495806.2:p.Ala150=
|
|
ENST00000155840.12:c.448G=
MANE Select
|
ENSP00000155840.2:p.Ala150=
|
|
ENST00000335475.6:c.67G=
|
ENSP00000334497.5:p.Ala23=
|
|
ENST00000646564.1:c.94G=
|
ENSP00000495806.1:p.Ala32=
|
|
ENST00000155840.9:c.448G=
|
ENSP00000155840.2:p.Ala150=
|
|
ENST00000335475.5:c.67G=
|
ENSP00000334497.5:p.Ala23=
|
|
ENST00000496887.6:c.187G=
|
ENSP00000434560.1:p.Ala63=
|
|
NM_000218.2:c.448G= , LRG_287t1:c.448G=
|
NP_000209.2:p.Ala150=
|
|
NM_181798.1:c.67G= , LRG_287t2:c.67G=
|
NP_861463.1:p.Ala23=
|
|
NM_000218.3:c.448G=
MANE Select
|
NP_000209.2:p.Ala150=
|
|