ENST00000321612.8:c.2002G=
MANE Select
|
ENSP00000370737.4:p.Val668=
|
|
ENST00000460457.2:n.162G=
|
|
|
ENST00000638233.1:n.437G=
|
|
|
ENST00000638661.1:c.202G=
|
ENSP00000491369.1:p.Val68=
|
|
ENST00000638694.1:n.189G=
|
|
|
ENST00000639318.1:c.202G=
|
ENSP00000491932.1:p.Val68=
|
|
ENST00000639364.1:n.1702G=
|
|
|
ENST00000639443.1:n.1570G=
|
|
|
ENST00000639954.1:n.1710G=
|
|
|
ENST00000640208.1:c.202G=
|
ENSP00000491895.1:p.Val68=
|
|
ENST00000640505.1:n.241G=
|
|
|
ENST00000640592.1:n.1885G=
|
|
|
ENST00000321612.6:c.2002G=
|
ENSP00000370737.3:p.Val668=
|
|
ENST00000460457.1:n.141G=
|
|
|
NM_000170.2:c.2002G= , LRG_643t1:c.2002G=
|
NP_000161.2:p.Val668=
|
|
NM_000170.3:c.2002G=
MANE Select
|
NP_000161.2:p.Val668=
|
|