ENST00000463045.3:c.-31G=
|
ENSP00000481376.2:n.-31G=
|
|
ENST00000491274.6:c.99G=
|
ENSP00000480482.2:p.Trp33=
|
|
ENST00000375499.8:c.141G=
MANE Select
|
ENSP00000364649.3:p.Trp47=
|
|
ENST00000375499.7:c.141G=
|
ENSP00000364649.3:p.Trp47=
|
|
ENST00000463045.2:c.-31G=
|
ENSP00000481376.1:n.-31G=
|
|
ENST00000466613.2:n.153G=
|
|
|
ENST00000475506.1:n.58G=
|
|
|
ENST00000485515.5:n.129G=
|
|
|
ENST00000491274.5:c.99G=
|
ENSP00000480482.1:p.Trp33=
|
|
NM_003000.2:c.141G= , LRG_316t1:c.141G=
|
NP_002991.2:p.Trp47=
|
|
NM_003000.3:c.141G=
MANE Select
|
NP_002991.2:p.Trp47=
|
|