ENST00000463045.3:c.-76T>A
|
ENSP00000481376.2:n.-76T>A
|
|
ENST00000491274.6:c.54T>A
|
ENSP00000480482.2:p.Ala18=
|
|
ENST00000375499.8:c.96T>A
MANE Select
|
ENSP00000364649.3:p.Ala32=
|
|
ENST00000375499.7:c.96T>A
|
ENSP00000364649.3:p.Ala32=
|
|
ENST00000463045.2:c.-76T>A
|
ENSP00000481376.1:n.-76T>A
|
|
ENST00000466613.2:n.108T>A
|
|
|
ENST00000475506.1:n.13T>A
|
|
|
ENST00000485515.5:n.84T>A
|
|
|
ENST00000491274.5:c.54T>A
|
ENSP00000480482.1:p.Ala18=
|
|
NM_003000.2:c.96T>A , LRG_316t1:c.96T>A
|
NP_002991.2:p.Ala32=
|
|
NM_003000.3:c.96T>A
MANE Select
|
NP_002991.2:p.Ala32=
|
|