ENST00000295408.9:c.588T>A
MANE Select
|
ENSP00000295408.4:p.Leu196=
|
|
ENST00000295408.8:c.588T>A
|
ENSP00000295408.4:p.Leu196=
|
|
ENST00000409780.5:c.60T>A
|
ENSP00000387277.1:p.Leu20=
|
|
ENST00000421804.6:c.588T>A
|
ENSP00000389152.2:p.Leu196=
|
|
ENST00000439966.5:c.*61T>A
|
ENSP00000402129.1:n.*61T>A
|
|
ENST00000616902.4:c.-628T>A
|
ENSP00000482824.1:n.-628T>A
|
|
NM_006343.2:c.588T>A
|
NP_006334.2:p.Leu196=
|
|
XM_005263565.3:c.588T>A
|
XP_005263622.1:p.Leu196=
|
|
XM_005263568.3:c.588T>A
|
XP_005263625.1:p.Leu196=
|
|
XM_011510490.1:c.399T>A
|
XP_011508792.1:p.Leu133=
|
|
XM_005263565.4:c.588T>A
|
XP_005263622.1:p.Leu196=
|
|
XM_005263568.4:c.588T>A
|
XP_005263625.1:p.Leu196=
|
|
XM_011510490.3:c.399T>A
|
XP_011508792.1:p.Leu133=
|
|
XM_017003164.1:c.399T>A
|
XP_016858653.1:p.Leu133=
|
|
XM_017003165.2:c.-680T>A
|
XP_016858654.1:n.-680T>A
|
|
NM_006343.3:c.588T>A
MANE Select
|
NP_006334.2:p.Leu196=
|
|