ENST00000371270.6:c.1459T>G
MANE Select
|
ENSP00000360317.3:p.Phe487Val
|
|
ENST00000371270.5:c.1459T>G
|
ENSP00000360317.3:p.Phe487Val
|
|
ENST00000490994.6:c.*1245T>G
|
ENSP00000433314.1:n.*1245T>G
|
|
ENST00000525991.5:c.*1034T>G
|
ENSP00000433842.1:n.*1034T>G
|
|
ENST00000526814.5:n.1714T>G
|
|
|
ENST00000527420.5:c.*316T>G
|
ENSP00000433191.1:n.*316T>G
|
|
ENST00000527953.5:n.1753T>G
|
|
|
ENST00000533320.5:n.1693T>G
|
|
|
ENST00000535898.5:c.1153T>G
|
ENSP00000445062.1:p.Phe385Val
|
|
ENST00000539050.5:c.1249T>G
|
ENSP00000442343.2:p.Phe417Val
|
|
ENST00000623108.3:c.1249T>G
|
ENSP00000485110.1:p.Phe417Val
|
|
NM_000770.3:c.1459T>G
MANE Select
|
NP_000761.3:p.Phe487Val
|
|
NM_001198853.1:c.1249T>G
|
NP_001185782.1:p.Phe417Val
|
|
NM_001198854.1:c.1153T>G
|
NP_001185783.1:p.Phe385Val
|
|
NM_001198855.1:c.1249T>G
|
NP_001185784.1:p.Phe417Val
|
|