ENST00000404922.8:c.3612C>G
MANE Select
|
ENSP00000384169.3:p.Asp1204Glu
|
|
ENST00000295760.11:c.3471C>G
|
ENSP00000295760.7:p.Asp1157Glu
|
|
ENST00000295761.11:c.254-262C>G
|
|
|
ENST00000404922.7:c.3612C>G
|
ENSP00000384169.3:p.Asp1204Glu
|
|
ENST00000421373.1:c.135+263C>G
|
|
|
ENST00000492059.5:c.3612C>G
|
ENSP00000420042.1:p.Asp1204Glu
|
|
NM_001004019.1:c.3612C>G
|
NP_001004019.1:p.Asp1204Glu
|
|
NM_001165035.1:c.3612C>G
|
NP_001158507.1:p.Asp1204Glu
|
|
NM_001998.2:c.3471C>G
|
NP_001989.2:p.Asp1157Glu
|
|
XM_006713026.2:c.3495C>G
|
XP_006713089.1:p.Asp1165Glu
|
|
NM_001004019.2:c.3612C>G
MANE Select
|
NP_001004019.1:p.Asp1204Glu
|
|
NM_001165035.2:c.3612C>G
|
NP_001158507.1:p.Asp1204Glu
|
|
NM_001998.3:c.3471C>G
|
NP_001989.2:p.Asp1157Glu
|
|