ENST00000324071.10:c.1166T>A
MANE Select
|
ENSP00000324648.2:p.Phe389Tyr
|
|
ENST00000598834.2:c.1176+202T>A
|
|
|
ENST00000324071.8:c.1166T>A
|
ENSP00000324648.2:p.Phe389Tyr
|
|
ENST00000593831.1:c.458T>A
|
ENSP00000470582.1:p.Phe153Tyr
|
|
ENST00000597612.1:n.647+202T>A
|
|
|
NM_000767.4:c.1166T>A
|
NP_000758.1:p.Phe389Tyr
|
|
XM_005258569.3:c.1152+202T>A
|
XP_005258626.1:n.1152+202T>A
|
|
XM_006723050.2:c.1166T>A
|
XP_006723113.1:p.Phe389Tyr
|
|
XM_011526546.1:c.1153-129T>A
|
XP_011524848.1:n.1153-129T>A
|
|
XM_011526547.1:c.1152+202T>A
|
XP_011524849.1:n.1152+202T>A
|
|
XM_011526548.1:c.686T>A
|
XP_011524850.1:p.Phe229Tyr
|
|
XM_011526549.1:c.575T>A
|
XP_011524851.1:p.Phe192Tyr
|
|
XM_011526550.1:c.566T>A
|
XP_011524852.1:p.Phe189Tyr
|
|
NM_000767.5:c.1166T>A
MANE Select
|
NP_000758.1:p.Phe389Tyr
|
|