ENST00000455537.7:c.2918A>T
MANE Select
|
ENSP00000408979.2:p.Asn973Ile
|
|
ENST00000674619.1:c.2939A>T
|
ENSP00000502270.1:p.Asn980Ile
|
|
ENST00000675697.1:c.9A>T
|
|
|
ENST00000675737.1:n.322A>T
|
|
|
ENST00000675882.1:n.2441A>T
|
|
|
ENST00000675929.1:n.1476A>T
|
|
|
ENST00000676055.1:c.9A>T
|
|
|
ENST00000676457.1:c.2813A>T
|
ENSP00000501588.1:p.Asn938Ile
|
|
ENST00000286452.5:c.2651A>T
|
ENSP00000286452.5:p.Asn884Ile
|
|
ENST00000455537.6:c.2918A>T
|
ENSP00000408979.2:p.Asn973Ile
|
|
ENST00000552227.1:n.201A>T
|
|
|
NM_004984.2:c.2918A>T
|
NP_004975.2:p.Asn973Ile
|
|
NM_001354705.1:c.2651A>T
|
NP_001341634.1:p.Asn884Ile
|
|
NM_004984.3:c.2918A>T
|
NP_004975.2:p.Asn973Ile
|
|
XR_002957324.1:n.3151A>T
|
|
|
NM_004984.4:c.2918A>T
MANE Select
|
NP_004975.2:p.Asn973Ile
|
|
NM_001354705.2:c.2651A>T
|
NP_001341634.1:p.Asn884Ile
|
|