ENST00000321612.8:c.2003T=
MANE Select
|
ENSP00000370737.4:p.Val668=
|
|
ENST00000460457.2:n.163T=
|
|
|
ENST00000638233.1:n.438T=
|
|
|
ENST00000638661.1:c.203T=
|
ENSP00000491369.1:p.Val68=
|
|
ENST00000638694.1:n.190T=
|
|
|
ENST00000639318.1:c.203T=
|
ENSP00000491932.1:p.Val68=
|
|
ENST00000639364.1:n.1703T=
|
|
|
ENST00000639443.1:n.1571T=
|
|
|
ENST00000639954.1:n.1711T=
|
|
|
ENST00000640208.1:c.203T=
|
ENSP00000491895.1:p.Val68=
|
|
ENST00000640505.1:n.242T=
|
|
|
ENST00000640592.1:n.1886T=
|
|
|
ENST00000321612.6:c.2003T=
|
ENSP00000370737.3:p.Val668=
|
|
ENST00000460457.1:n.142T=
|
|
|
NM_000170.2:c.2003T= , LRG_643t1:c.2003T=
|
NP_000161.2:p.Val668=
|
|
NM_000170.3:c.2003T=
MANE Select
|
NP_000161.2:p.Val668=
|
|