ENST00000321612.8:c.2071A>T
MANE Select
|
ENSP00000370737.4:p.Asn691Tyr
|
|
ENST00000638233.1:n.506A>T
|
|
|
ENST00000638661.1:c.271A>T
|
ENSP00000491369.1:p.Asn91Tyr
|
|
ENST00000638694.1:n.258A>T
|
|
|
ENST00000639318.1:c.271A>T
|
ENSP00000491932.1:p.Asn91Tyr
|
|
ENST00000639364.1:n.1771A>T
|
|
|
ENST00000639443.1:n.1639A>T
|
|
|
ENST00000639954.1:n.1779A>T
|
|
|
ENST00000640505.1:n.310A>T
|
|
|
ENST00000321612.6:c.2071A>T
|
ENSP00000370737.3:p.Asn691Tyr
|
|
NM_000170.2:c.2071A>T , LRG_643t1:c.2071A>T
|
NP_000161.2:p.Asn691Tyr
|
|
NM_000170.3:c.2071A>T
MANE Select
|
NP_000161.2:p.Asn691Tyr
|
|