ENST00000281928.9:c.5127A>C
MANE Select
|
ENSP00000281928.3:p.Glu1709Asp
|
|
ENST00000549786.2:c.4555A>C
|
|
|
ENST00000648379.1:n.3495A>C
|
|
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ENST00000648737.1:n.4891A>C
|
|
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ENST00000648825.1:n.1867A>C
|
|
|
ENST00000648916.1:n.3138A>C
|
|
|
ENST00000649146.1:n.2370A>C
|
|
|
ENST00000649607.1:c.3311A>C
|
|
|
ENST00000649775.1:c.1616A>C
|
|
|
ENST00000650226.1:c.5127A>C
|
ENSP00000496981.1:p.Glu1709Asp
|
|
ENST00000281928.7:c.5127A>C
|
ENSP00000281928.3:p.Glu1709Asp
|
|
ENST00000549786.1:c.491A>C
|
|
|
ENST00000552340.1:c.159A>C
|
ENSP00000449876.1:p.Glu53Asp
|
|
NM_015335.4:c.5127A>C
|
NP_056150.1:p.Glu1709Asp
|
|
XM_011538080.1:c.5127A>C
|
XP_011536382.1:p.Glu1709Asp
|
|
XM_011538081.1:c.5124A>C
|
XP_011536383.1:p.Glu1708Asp
|
|
XM_011538082.1:c.5097A>C
|
XP_011536384.1:p.Glu1699Asp
|
|
XM_011538080.2:c.5127A>C
|
XP_011536382.1:p.Glu1709Asp
|
|
XM_011538081.2:c.5124A>C
|
XP_011536383.1:p.Glu1708Asp
|
|
XM_011538082.2:c.5097A>C
|
XP_011536384.1:p.Glu1699Asp
|
|
XM_017019090.1:c.5124A>C
|
XP_016874579.1:p.Glu1708Asp
|
|
NM_015335.5:c.5127A>C
MANE Select
|
NP_056150.1:p.Glu1709Asp
|
|