ENST00000324071.10:c.1286T>A
MANE Select
|
ENSP00000324648.2:p.Phe429Tyr
|
|
ENST00000598834.2:c.1177-166T>A
|
|
|
ENST00000324071.8:c.1286T>A
|
ENSP00000324648.2:p.Phe429Tyr
|
|
ENST00000593831.1:c.578T>A
|
ENSP00000470582.1:p.Phe193Tyr
|
|
ENST00000597612.1:n.647+322T>A
|
|
|
NM_000767.4:c.1286T>A
|
NP_000758.1:p.Phe429Tyr
|
|
XM_005258569.3:c.1152+322T>A
|
XP_005258626.1:n.1152+322T>A
|
|
XM_006723050.2:c.1286T>A
|
XP_006723113.1:p.Phe429Tyr
|
|
XM_011526546.1:c.1153-9T>A
|
XP_011524848.1:n.1153-9T>A
|
|
XM_011526547.1:c.1153-166T>A
|
XP_011524849.1:n.1153-166T>A
|
|
XM_011526548.1:c.806T>A
|
XP_011524850.1:p.Phe269Tyr
|
|
XM_011526549.1:c.695T>A
|
XP_011524851.1:p.Phe232Tyr
|
|
XM_011526550.1:c.686T>A
|
XP_011524852.1:p.Phe229Tyr
|
|
NM_000767.5:c.1286T>A
MANE Select
|
NP_000758.1:p.Phe429Tyr
|
|