ENST00000321612.8:c.2050A=
MANE Select
|
ENSP00000370737.4:p.Met684=
|
|
ENST00000460457.2:n.210A=
|
|
|
ENST00000638233.1:n.485A=
|
|
|
ENST00000638661.1:c.250A=
|
ENSP00000491369.1:p.Met84=
|
|
ENST00000638694.1:n.237A=
|
|
|
ENST00000639318.1:c.250A=
|
ENSP00000491932.1:p.Met84=
|
|
ENST00000639364.1:n.1750A=
|
|
|
ENST00000639443.1:n.1618A=
|
|
|
ENST00000639954.1:n.1758A=
|
|
|
ENST00000640208.1:c.250A=
|
ENSP00000491895.1:p.Met84=
|
|
ENST00000640505.1:n.289A=
|
|
|
ENST00000640592.1:n.1933A=
|
|
|
ENST00000321612.6:c.2050A=
|
ENSP00000370737.3:p.Met684=
|
|
ENST00000460457.1:n.189A=
|
|
|
NM_000170.2:c.2050A= , LRG_643t1:c.2050A=
|
NP_000161.2:p.Met684=
|
|
NM_000170.3:c.2050A=
MANE Select
|
NP_000161.2:p.Met684=
|
|