ENST00000290866.10:c.312G>T
MANE Select
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ENSP00000290866.4:p.Leu104=
|
|
ENST00000290866.9:c.312G>T
|
ENSP00000290866.4:p.Leu104=
|
|
ENST00000428043.5:c.312G>T
|
ENSP00000397593.2:p.Leu104=
|
|
ENST00000579462.1:n.337G>T
|
|
|
ENST00000580318.1:n.501G>T
|
|
|
ENST00000582627.1:c.312G>T
|
ENSP00000462280.1:p.Leu104=
|
|
ENST00000582678.5:c.312G>T
|
ENSP00000462995.1:p.Leu104=
|
|
ENST00000583336.5:n.346G>T
|
|
|
ENST00000584529.5:n.346G>T
|
|
|
NM_000789.3:c.312G>T
|
NP_000780.1:p.Leu104=
|
|
XM_005257110.1:c.-144G>T
|
XP_005257167.1:n.-144G>T
|
|
NM_000789.4:c.312G>T
MANE Select
|
NP_000780.1:p.Leu104=
|
|
NM_001382700.1:c.77G>T
|
NP_001369629.1:p.Cys26Phe
|
|
NM_001382701.1:c.-303G>T
|
NP_001369630.1:n.-303G>T
|
|