ENST00000324071.10:c.1024G>T
MANE Select
|
ENSP00000324648.2:p.Asp342Tyr
|
|
ENST00000598834.2:c.1048G>T
|
|
|
ENST00000324071.8:c.1024G>T
|
ENSP00000324648.2:p.Asp342Tyr
|
|
ENST00000593831.1:c.316G>T
|
ENSP00000470582.1:p.Asp106Tyr
|
|
ENST00000597612.1:n.519G>T
|
|
|
NM_000767.4:c.1024G>T
|
NP_000758.1:p.Asp342Tyr
|
|
XM_005258569.3:c.1024G>T
|
XP_005258626.1:p.Asp342Tyr
|
|
XM_006723050.2:c.1024G>T
|
XP_006723113.1:p.Asp342Tyr
|
|
XM_011526546.1:c.1024G>T
|
XP_011524848.1:p.Asp342Tyr
|
|
XM_011526547.1:c.1024G>T
|
XP_011524849.1:p.Asp342Tyr
|
|
XM_011526548.1:c.544G>T
|
XP_011524850.1:p.Asp182Tyr
|
|
XM_011526549.1:c.433G>T
|
XP_011524851.1:p.Asp145Tyr
|
|
XM_011526550.1:c.424G>T
|
XP_011524852.1:p.Asp142Tyr
|
|
NM_000767.5:c.1024G>T
MANE Select
|
NP_000758.1:p.Asp342Tyr
|
|