ENST00000349748.8:c.1159G>A
|
ENSP00000183936.4:p.Glu387Lys
|
|
ENST00000357568.8:c.1303G>A
|
ENSP00000350181.3:p.Glu435Lys
|
|
ENST00000397163.8:c.1303G>A
MANE Select
|
ENSP00000380349.3:p.Glu435Lys
|
|
ENST00000466369.5:n.1812G>A
|
|
|
ENST00000483208.5:n.1534G>A
|
|
|
ENST00000495723.1:n.1534G>A
|
|
|
ENST00000549793.5:n.1534G>A
|
|
|
ENST00000638141.2:n.1174G>A
|
|
|
ENST00000673658.1:n.287G>A
|
|
|
ENST00000673705.1:c.258G>A
|
ENSP00000501021.1:n.258G>A
|
|
ENST00000318023.11:c.1159G>A
|
ENSP00000326281.8:p.Glu387Lys
|
|
ENST00000349748.7:c.1159G>A
|
ENSP00000183936.4:p.Glu387Lys
|
|
ENST00000357568.7:c.1303G>A
|
ENSP00000350181.3:p.Glu435Lys
|
|
ENST00000397163.7:c.1303G>A
|
ENSP00000380349.3:p.Glu435Lys
|
|
NM_000070.2:c.1303G>A
|
NP_000061.1:p.Glu435Lys
|
|
NM_024344.1:c.1303G>A
|
NP_077320.1:p.Glu435Lys
|
|
NM_173087.1:c.1159G>A
|
NP_775110.1:p.Glu387Lys
|
|
NM_000070.3:c.1303G>A
MANE Select
|
NP_000061.1:p.Glu435Lys
|
|
NM_024344.2:c.1303G>A
|
NP_077320.1:p.Glu435Lys
|
|
NM_173087.2:c.1159G>A
|
NP_775110.1:p.Glu387Lys
|
|