ENST00000318312.12:c.313G=
MANE Select
|
ENSP00000317469.7:p.Ala105=
|
|
ENST00000318312.11:c.313G=
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ENSP00000317469.7:p.Ala105=
|
|
ENST00000393994.4:c.313G=
|
ENSP00000377563.2:p.Ala105=
|
|
ENST00000419755.3:c.424G=
|
ENSP00000398526.3:p.Ala142=
|
|
ENST00000455748.6:c.313G=
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ENSP00000405764.2:p.Ala105=
|
|
ENST00000524458.5:c.*20G=
|
ENSP00000436195.1:n.*20G=
|
|
ENST00000524705.2:c.34G=
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ENSP00000436927.1:p.Ala12=
|
|
ENST00000524907.5:n.303G=
|
|
|
ENST00000525809.5:c.160-981G=
|
ENSP00000431187.1:n.160-981G=
|
|
ENST00000526035.5:c.*20G=
|
ENSP00000434197.1:n.*20G=
|
|
ENST00000526760.5:c.*20G=
|
ENSP00000432140.1:n.*20G=
|
|
ENST00000527251.5:c.*20G=
|
ENSP00000434360.1:n.*20G=
|
|
ENST00000529766.5:n.320G=
|
|
|
ENST00000529955.5:n.331G=
|
|
|
ENST00000532908.5:c.*20G=
|
ENSP00000431866.1:n.*20G=
|
|
ENST00000533430.5:n.91G=
|
|
|
ENST00000533557.5:c.*20G=
|
ENSP00000434619.1:n.*20G=
|
|
ENST00000533644.5:c.313G=
|
ENSP00000436073.1:p.Ala105=
|
|
ENST00000534730.5:n.325G=
|
|
|
ENST00000630659.2:c.*20G=
|
ENSP00000486455.1:n.*20G=
|
|
NM_024649.4:c.313G=
|
NP_078925.3:p.Ala105=
|
|
NM_024649.5:c.313G=
MANE Select
|
NP_078925.3:p.Ala105=
|
|