NM_000170.3:c.2216G=
MANE Select
|
NP_000161.2:p.Arg739=
|
ENST00000321612.8:c.2216G=
MANE Select
|
ENSP00000370737.4:p.Arg739=
|
NM_000170.2:c.2216G= , LRG_643t1:c.2216G=
|
NP_000161.2:p.Arg739=
|
ENST00000321612.6:c.2216G=
|
ENSP00000370737.3:p.Arg739=
|
ENST00000467946.1:n.142G=
|
|
ENST00000638233.1:n.651G=
|
|
ENST00000638661.1:c.416G=
|
ENSP00000491369.1:p.Arg139=
|
ENST00000638694.1:n.403G=
|
|
ENST00000639318.1:c.416G=
|
ENSP00000491932.1:p.Arg139=
|
ENST00000639364.1:n.1916G=
|
|
ENST00000639443.1:n.1784G=
|
|
ENST00000639639.1:c.-83G=
|
ENSP00000491312.1:n.-83G=
|
ENST00000639954.1:n.1924G=
|
|
ENST00000640505.1:n.455G=
|
|