ENST00000393931.8:c.2221G>T
MANE Select
|
ENSP00000377508.3:p.Asp741Tyr
|
|
ENST00000310706.9:c.2221G>T
|
ENSP00000311113.5:p.Asp741Tyr
|
|
ENST00000393930.5:c.2221G>T
|
ENSP00000377507.1:p.Asp741Tyr
|
|
ENST00000393931.7:c.2221G>T
|
ENSP00000377508.3:p.Asp741Tyr
|
|
NM_002230.2:c.2221G>T , LRG_401t2:c.2221G>T
|
NP_002221.1:p.Asp741Tyr
|
|
NM_021991.2:c.2221G>T , LRG_401t1:c.2221G>T
|
NP_068831.1:p.Asp741Tyr
|
|
XM_006721873.1:c.2221G>T
|
XP_006721936.1:p.Asp741Tyr
|
|
XM_006721874.1:c.2221G>T
|
XP_006721937.1:p.Asp741Tyr
|
|
XM_006721875.1:c.2221G>T
|
XP_006721938.1:p.Asp741Tyr
|
|
XM_006721878.1:c.2221G>T
|
XP_006721941.1:p.Asp741Tyr
|
|
XM_011524753.1:c.2221G>T
|
XP_011523055.1:p.Asp741Tyr
|
|
XM_011524754.1:c.2221G>T
|
XP_011523056.1:p.Asp741Tyr
|
|
XM_011524755.1:c.2221G>T
|
XP_011523057.1:p.Asp741Tyr
|
|
XM_011524756.1:c.2221G>T
|
XP_011523058.1:p.Asp741Tyr
|
|
XM_011524757.1:c.2221G>T
|
XP_011523059.1:p.Asp741Tyr
|
|
XM_011524758.1:c.2221G>T
|
XP_011523060.1:p.Asp741Tyr
|
|
NM_001352773.1:c.2221G>T
|
NP_001339702.1:p.Asp741Tyr
|
|
NM_001352774.1:c.2221G>T
|
NP_001339703.1:p.Asp741Tyr
|
|
NM_001352775.1:c.2221G>T
|
NP_001339704.1:p.Asp741Tyr
|
|
NM_001352776.1:c.2221G>T
|
NP_001339705.1:p.Asp741Tyr
|
|
NM_001352777.1:c.2221G>T
|
NP_001339706.1:p.Asp741Tyr
|
|
NM_002230.3:c.2221G>T
|
NP_002221.1:p.Asp741Tyr
|
|
NM_021991.3:c.2221G>T
|
NP_068831.1:p.Asp741Tyr
|
|
XM_006721874.3:c.2221G>T
|
XP_006721937.1:p.Asp741Tyr
|
|
XM_011524753.2:c.2221G>T
|
XP_011523055.1:p.Asp741Tyr
|
|
XM_017024588.2:c.2272G>T
|
XP_016880077.1:p.Asp758Tyr
|
|
XM_017024590.1:c.2221G>T
|
XP_016880079.1:p.Asp741Tyr
|
|
NM_002230.4:c.2221G>T
MANE Select
|
NP_002221.1:p.Asp741Tyr
|
|
NM_001352773.2:c.2221G>T
|
NP_001339702.1:p.Asp741Tyr
|
|
NM_001352774.2:c.2221G>T
|
NP_001339703.1:p.Asp741Tyr
|
|
NM_001352775.2:c.2221G>T
|
NP_001339704.1:p.Asp741Tyr
|
|
NM_001352776.2:c.2221G>T
|
NP_001339705.1:p.Asp741Tyr
|
|
NM_001352777.2:c.2221G>T
|
NP_001339706.1:p.Asp741Tyr
|
|
NM_021991.4:c.2221G>T
|
NP_068831.1:p.Asp741Tyr
|
|