ENST00000321612.8:c.2152C>T
MANE Select
|
ENSP00000370737.4:p.His718Tyr
|
|
ENST00000638233.1:n.587C>T
|
|
|
ENST00000638661.1:c.352C>T
|
ENSP00000491369.1:p.His118Tyr
|
|
ENST00000638694.1:n.339C>T
|
|
|
ENST00000639318.1:c.352C>T
|
ENSP00000491932.1:p.His118Tyr
|
|
ENST00000639364.1:n.1852C>T
|
|
|
ENST00000639443.1:n.1720C>T
|
|
|
ENST00000639954.1:n.1860C>T
|
|
|
ENST00000640505.1:n.391C>T
|
|
|
ENST00000321612.6:c.2152C>T
|
ENSP00000370737.3:p.His718Tyr
|
|
NM_000170.2:c.2152C>T , LRG_643t1:c.2152C>T
|
NP_000161.2:p.His718Tyr
|
|
NM_000170.3:c.2152C>T
MANE Select
|
NP_000161.2:p.His718Tyr
|
|