ENST00000584880.6:c.*386A>G
|
ENSP00000464347.2:n.*386A>G
|
|
ENST00000703608.1:c.*706A>G
|
ENSP00000515392.1:n.*706A>G
|
|
ENST00000703609.1:c.1108A>G
|
ENSP00000515393.1:p.Lys370Glu
|
|
ENST00000703610.1:c.*466A>G
|
ENSP00000515394.1:n.*466A>G
|
|
ENST00000310144.11:c.1189A>G
MANE Select
|
ENSP00000310572.6:p.Lys397Glu
|
|
ENST00000310144.10:c.1189A>G
|
ENSP00000310572.6:p.Lys397Glu
|
|
ENST00000375812.8:c.1165A>G
|
ENSP00000364970.4:p.Lys389Glu
|
|
ENST00000578570.5:n.1599A>G
|
|
|
ENST00000579147.5:n.2504A>G
|
|
|
ENST00000580864.5:c.1165A>G
|
ENSP00000462495.1:p.Lys389Glu
|
|
ENST00000581882.5:c.1165A>G
|
ENSP00000463938.1:p.Lys389Glu
|
|
ENST00000584657.1:n.494A>G
|
|
|
ENST00000585242.5:c.*960A>G
|
ENSP00000463107.1:n.*960A>G
|
|
NM_001199163.1:c.1165A>G
|
NP_001186092.1:p.Lys389Glu
|
|
NM_002805.5:c.1189A>G
|
NP_002796.4:p.Lys397Glu
|
|
XM_006721980.1:c.1189A>G
|
XP_006722043.1:p.Lys397Glu
|
|
XR_934508.1:n.1278A>G
|
|
|
XM_024450840.1:c.1270A>G
|
XP_024306608.1:p.Lys424Glu
|
|
XM_024450841.1:c.1246A>G
|
XP_024306609.1:p.Lys416Glu
|
|
XR_934508.2:n.1265A>G
|
|
|
NM_002805.6:c.1189A>G
MANE Select
|
NP_002796.4:p.Lys397Glu
|
|
NM_001199163.2:c.1165A>G
|
NP_001186092.1:p.Lys389Glu
|
|