ENST00000463045.3:c.115G=
|
ENSP00000481376.2:p.Gly39=
|
|
ENST00000491274.6:c.244G=
|
ENSP00000480482.2:p.Gly82=
|
|
ENST00000375499.8:c.286G=
MANE Select
|
ENSP00000364649.3:p.Gly96=
|
|
ENST00000375499.7:c.286G=
|
ENSP00000364649.3:p.Gly96=
|
|
ENST00000463045.2:c.115G=
|
ENSP00000481376.1:p.Gly39=
|
|
ENST00000466613.2:n.298G=
|
|
|
ENST00000475506.1:n.203G=
|
|
|
ENST00000485515.5:n.274G=
|
|
|
ENST00000491274.5:c.244G=
|
ENSP00000480482.1:p.Gly82=
|
|
NM_003000.2:c.286G= , LRG_316t1:c.286G=
|
NP_002991.2:p.Gly96=
|
|
NM_003000.3:c.286G=
MANE Select
|
NP_002991.2:p.Gly96=
|
|