ENST00000682785.1:n.572T>A
|
|
|
ENST00000264896.8:c.596T>A
MANE Select
|
ENSP00000264896.2:p.Phe199Tyr
|
|
ENST00000502908.2:n.2097T>A
|
|
|
ENST00000638295.1:c.122T>A
|
ENSP00000492288.1:p.Phe41Tyr
|
|
ENST00000638372.1:n.848T>A
|
|
|
ENST00000638603.1:c.596T>A
|
ENSP00000491728.1:p.Phe199Tyr
|
|
ENST00000638663.1:c.596T>A
|
ENSP00000491407.1:p.Phe199Tyr
|
|
ENST00000638680.1:n.2177T>A
|
|
|
ENST00000639145.1:c.587T>A
|
ENSP00000492831.1:p.Phe196Tyr
|
|
ENST00000639300.1:c.596T>A
|
ENSP00000492840.1:p.Phe199Tyr
|
|
ENST00000639324.1:n.695T>A
|
|
|
ENST00000639715.1:c.551T>A
|
|
|
ENST00000639738.1:c.276-13232T>A
|
ENSP00000491792.1:n.276-13232T>A
|
|
ENST00000640076.1:n.177T>A
|
|
|
ENST00000640341.1:c.*236T>A
|
ENSP00000492714.1:n.*236T>A
|
|
ENST00000640634.1:c.717T>A
|
|
|
ENST00000640640.1:c.596T>A
|
ENSP00000492246.1:p.Phe199Tyr
|
|
ENST00000640916.1:n.524T>A
|
|
|
ENST00000640957.1:c.596T>A
|
ENSP00000492004.1:p.Phe199Tyr
|
|
ENST00000264896.6:c.596T>A
|
ENSP00000264896.2:p.Phe199Tyr
|
|
ENST00000452464.6:c.276-3623T>A
|
ENSP00000399154.2:n.276-3623T>A
|
|
NM_001204255.1:c.276-3623T>A
|
NP_001191184.1:n.276-3623T>A
|
|
NM_005506.3:c.596T>A
|
NP_005497.1:p.Phe199Tyr
|
|
NM_005506.4:c.596T>A
MANE Select
|
NP_005497.1:p.Phe199Tyr
|
|
NM_001204255.2:c.276-3623T>A
|
NP_001191184.1:n.276-3623T>A
|
|