ENST00000557912.2:c.96T>G
|
ENSP00000453475.1:p.Ala32=
|
|
ENST00000699926.1:c.157T>G
|
ENSP00000514692.1:p.Phe53Val
|
|
ENST00000699934.1:c.154T>G
|
ENSP00000514697.1:p.Phe52Val
|
|
ENST00000699935.1:c.178T>G
|
ENSP00000514698.1:p.Phe60Val
|
|
ENST00000699936.1:c.88T>G
|
ENSP00000514699.1:p.Phe30Val
|
|
ENST00000699937.1:c.139T>G
|
ENSP00000514700.1:p.Phe47Val
|
|
ENST00000699938.1:c.154T>G
|
ENSP00000514701.1:p.Phe52Val
|
|
ENST00000699939.1:n.301T>G
|
|
|
ENST00000328848.6:c.154T>G
MANE Select
|
ENSP00000332198.5:p.Phe52Val
|
|
ENST00000328848.5:c.154T>G
|
ENSP00000332198.4:p.Phe52Val
|
|
ENST00000557912.1:c.96T>G
|
ENSP00000453475.1:p.Ala32=
|
|
NM_018648.3:c.154T>G , LRG_345t1:c.154T>G
|
NP_061118.1:p.Phe52Val
|
|
NM_018648.4:c.154T>G
MANE Select
|
NP_061118.1:p.Phe52Val
|
|