ENST00000463045.3:c.348C>A
|
ENSP00000481376.2:p.Ser116=
|
|
ENST00000491274.6:c.477C>A
|
ENSP00000480482.2:p.Ser159=
|
|
ENST00000375499.8:c.519C>A
MANE Select
|
ENSP00000364649.3:p.Ser173=
|
|
ENST00000375499.7:c.519C>A
|
ENSP00000364649.3:p.Ser173=
|
|
ENST00000463045.2:c.348C>A
|
ENSP00000481376.1:p.Ser116=
|
|
ENST00000475506.1:n.436C>A
|
|
|
ENST00000485515.5:n.453C>A
|
|
|
ENST00000491274.5:c.477C>A
|
ENSP00000480482.1:p.Ser159=
|
|
NM_003000.2:c.519C>A , LRG_316t1:c.519C>A
|
NP_002991.2:p.Ser173=
|
|
NM_003000.3:c.519C>A
MANE Select
|
NP_002991.2:p.Ser173=
|
|