ENST00000450114.7:c.1428A>C
MANE Select
|
ENSP00000402084.2:p.Glu476Asp
|
|
ENST00000530712.6:c.246A>C
|
ENSP00000434148.2:p.Glu82Asp
|
|
ENST00000680141.1:c.*378A>C
|
ENSP00000506686.1:n.*378A>C
|
|
ENST00000681684.1:c.786A>C
|
ENSP00000506667.1:p.Glu262Asp
|
|
ENST00000299613.10:c.786A>C
|
ENSP00000299613.5:p.Glu262Asp
|
|
ENST00000450114.6:c.1428A>C
|
ENSP00000402084.2:p.Glu476Asp
|
|
ENST00000524612.5:c.312A>C
|
ENSP00000434446.1:p.Glu104Asp
|
|
ENST00000530175.5:c.275A>C
|
|
|
ENST00000530712.5:c.246A>C
|
ENSP00000434148.1:p.Glu82Asp
|
|
ENST00000532275.1:n.215A>C
|
|
|
NM_001143976.1:c.786A>C
|
NP_001137448.1:p.Glu262Asp
|
|
NM_003390.3:c.1428A>C
|
NP_003381.1:p.Glu476Asp
|
|
XM_005253118.3:c.1428A>C
|
XP_005253175.1:p.Glu476Asp
|
|
XM_005253119.3:c.786A>C
|
XP_005253176.1:p.Glu262Asp
|
|
NM_003390.4:c.1428A>C
MANE Select
|
NP_003381.1:p.Glu476Asp
|
|
NM_001143976.2:c.786A>C
|
NP_001137448.1:p.Glu262Asp
|
|