ENST00000324071.10:c.796G>T
MANE Select
|
ENSP00000324648.2:p.Asp266Tyr
|
|
ENST00000598834.2:c.820G>T
|
|
|
ENST00000324071.8:c.796G>T
|
ENSP00000324648.2:p.Asp266Tyr
|
|
ENST00000593831.1:c.257-2929G>T
|
ENSP00000470582.1:n.257-2929G>T
|
|
NM_000767.4:c.796G>T
|
NP_000758.1:p.Asp266Tyr
|
|
XM_005258569.3:c.796G>T
|
XP_005258626.1:p.Asp266Tyr
|
|
XM_006723050.2:c.796G>T
|
XP_006723113.1:p.Asp266Tyr
|
|
XM_011526546.1:c.796G>T
|
XP_011524848.1:p.Asp266Tyr
|
|
XM_011526547.1:c.796G>T
|
XP_011524849.1:p.Asp266Tyr
|
|
XM_011526548.1:c.485-2929G>T
|
XP_011524850.1:n.485-2929G>T
|
|
XM_011526549.1:c.205G>T
|
XP_011524851.1:p.Asp69Tyr
|
|
XM_011526550.1:c.365-2929G>T
|
XP_011524852.1:n.365-2929G>T
|
|
NM_000767.5:c.796G>T
MANE Select
|
NP_000758.1:p.Asp266Tyr
|
|