ENST00000257895.10:c.315T>A
MANE Select
|
ENSP00000257895.6:p.Leu105=
|
|
ENST00000257895.9:c.315T>A
|
ENSP00000257895.5:p.Leu105=
|
|
ENST00000257899.3:c.330T>A
|
|
|
ENST00000547072.5:c.24T>A
|
ENSP00000449927.1:p.Leu8=
|
|
ENST00000547301.1:n.423T>A
|
|
|
ENST00000548082.1:c.315T>A
|
ENSP00000447128.1:p.Leu105=
|
|
ENST00000548123.1:c.300+199T>A
|
|
|
ENST00000548486.1:n.325T>A
|
|
|
ENST00000549424.1:c.122T>A
|
ENSP00000447621.1:p.Phe41Tyr
|
|
ENST00000550412.5:c.356T>A
|
ENSP00000447650.1:p.Phe119Tyr
|
|
ENST00000550608.1:n.454T>A
|
|
|
ENST00000551946.5:c.*118T>A
|
ENSP00000450201.1:n.*118T>A
|
|
ENST00000552930.5:c.24T>A
|
ENSP00000448014.1:p.Leu8=
|
|
ENST00000553160.1:n.406-502T>A
|
|
|
ENST00000553187.5:n.325T>A
|
|
|
NM_001199771.1:c.315T>A
|
NP_001186700.1:p.Leu105=
|
|
NM_002905.3:c.315T>A
|
NP_002896.2:p.Leu105=
|
|
NR_037658.1:n.374T>A
|
|
|
NM_001199771.2:c.315T>A
|
NP_001186700.1:p.Leu105=
|
|
NM_002905.5:c.315T>A
MANE Select
|
NP_002896.2:p.Leu105=
|
|
NM_001199771.3:c.315T>A
|
NP_001186700.1:p.Leu105=
|
|