ENST00000496887.7:c.200G=
|
ENSP00000434560.2:p.Gly67=
|
|
ENST00000646564.2:c.461G=
|
ENSP00000495806.2:p.Gly154=
|
|
ENST00000155840.12:c.461G=
MANE Select
|
ENSP00000155840.2:p.Gly154=
|
|
ENST00000335475.6:c.80G=
|
ENSP00000334497.5:p.Gly27=
|
|
ENST00000646564.1:c.107G=
|
ENSP00000495806.1:p.Gly36=
|
|
ENST00000155840.9:c.461G=
|
ENSP00000155840.2:p.Gly154=
|
|
ENST00000335475.5:c.80G=
|
ENSP00000334497.5:p.Gly27=
|
|
ENST00000496887.6:c.200G=
|
ENSP00000434560.1:p.Gly67=
|
|
NM_000218.2:c.461G= , LRG_287t1:c.461G=
|
NP_000209.2:p.Gly154=
|
|
NM_181798.1:c.80G= , LRG_287t2:c.80G=
|
NP_861463.1:p.Gly27=
|
|
NM_000218.3:c.461G=
MANE Select
|
NP_000209.2:p.Gly154=
|
|