ENST00000324071.10:c.1269T>A
MANE Select
|
ENSP00000324648.2:p.Thr423=
|
|
ENST00000598834.2:c.1177-183T>A
|
|
|
ENST00000324071.8:c.1269T>A
|
ENSP00000324648.2:p.Thr423=
|
|
ENST00000593831.1:c.561T>A
|
ENSP00000470582.1:p.Thr187=
|
|
ENST00000597612.1:n.647+305T>A
|
|
|
NM_000767.4:c.1269T>A
|
NP_000758.1:p.Thr423=
|
|
XM_005258569.3:c.1152+305T>A
|
XP_005258626.1:n.1152+305T>A
|
|
XM_006723050.2:c.1269T>A
|
XP_006723113.1:p.Thr423=
|
|
XM_011526546.1:c.1153-26T>A
|
XP_011524848.1:n.1153-26T>A
|
|
XM_011526547.1:c.1153-183T>A
|
XP_011524849.1:n.1153-183T>A
|
|
XM_011526548.1:c.789T>A
|
XP_011524850.1:p.Thr263=
|
|
XM_011526549.1:c.678T>A
|
XP_011524851.1:p.Thr226=
|
|
XM_011526550.1:c.669T>A
|
XP_011524852.1:p.Thr223=
|
|
NM_000767.5:c.1269T>A
MANE Select
|
NP_000758.1:p.Thr423=
|
|