ENST00000426263.10:c.708C>G
MANE Select
|
ENSP00000416293.2:p.Asp236Glu
|
|
ENST00000669445.1:c.57-19C>G
|
|
|
ENST00000674765.1:c.708C>G
|
ENSP00000501811.1:p.Asp236Glu
|
|
ENST00000675112.1:n.731C>G
|
|
|
ENST00000676254.1:n.1157C>G
|
|
|
ENST00000426263.7:c.708C>G
|
ENSP00000416293.2:p.Asp236Glu
|
|
ENST00000439722.2:c.587C>G
|
ENSP00000395521.2:n.587C>G
|
|
ENST00000475162.3:c.415+874C>G
|
|
|
ENST00000630287.2:c.*23C>G
|
ENSP00000486694.1:n.*23C>G
|
|
NM_006516.2:c.708C>G
|
NP_006507.2:p.Asp236Glu
|
|
NM_006516.3:c.708C>G
|
NP_006507.2:p.Asp236Glu
|
|
NM_006516.4:c.708C>G
MANE Select
|
NP_006507.2:p.Asp236Glu
|
|