ENST00000324071.10:c.998G>A
MANE Select
|
ENSP00000324648.2:p.Gly333Asp
|
|
ENST00000598834.2:c.1022G>A
|
|
|
ENST00000324071.8:c.998G>A
|
ENSP00000324648.2:p.Gly333Asp
|
|
ENST00000593831.1:c.290G>A
|
ENSP00000470582.1:p.Gly97Asp
|
|
ENST00000597612.1:n.493G>A
|
|
|
NM_000767.4:c.998G>A
|
NP_000758.1:p.Gly333Asp
|
|
XM_005258569.3:c.998G>A
|
XP_005258626.1:p.Gly333Asp
|
|
XM_006723050.2:c.998G>A
|
XP_006723113.1:p.Gly333Asp
|
|
XM_011526546.1:c.998G>A
|
XP_011524848.1:p.Gly333Asp
|
|
XM_011526547.1:c.998G>A
|
XP_011524849.1:p.Gly333Asp
|
|
XM_011526548.1:c.518G>A
|
XP_011524850.1:p.Gly173Asp
|
|
XM_011526549.1:c.407G>A
|
XP_011524851.1:p.Gly136Asp
|
|
XM_011526550.1:c.398G>A
|
XP_011524852.1:p.Gly133Asp
|
|
NM_000767.5:c.998G>A
MANE Select
|
NP_000758.1:p.Gly333Asp
|
|