ENST00000463045.3:c.-73A>T
|
ENSP00000481376.2:n.-73A>T
|
|
ENST00000491274.6:c.57A>T
|
ENSP00000480482.2:p.Ala19=
|
|
ENST00000375499.8:c.99A>T
MANE Select
|
ENSP00000364649.3:p.Ala33=
|
|
ENST00000375499.7:c.99A>T
|
ENSP00000364649.3:p.Ala33=
|
|
ENST00000463045.2:c.-73A>T
|
ENSP00000481376.1:n.-73A>T
|
|
ENST00000466613.2:n.111A>T
|
|
|
ENST00000475506.1:n.16A>T
|
|
|
ENST00000485515.5:n.87A>T
|
|
|
ENST00000491274.5:c.57A>T
|
ENSP00000480482.1:p.Ala19=
|
|
NM_003000.2:c.99A>T , LRG_316t1:c.99A>T
|
NP_002991.2:p.Ala33=
|
|
NM_003000.3:c.99A>T
MANE Select
|
NP_002991.2:p.Ala33=
|
|