ENST00000369047.9:c.406G>C
MANE Select
|
ENSP00000358043.4:p.Asp136His
|
|
ENST00000346569.6:c.406G>C
|
ENSP00000271630.6:p.Asp136His
|
|
ENST00000369047.8:c.406G>C
|
ENSP00000358043.4:p.Asp136His
|
|
ENST00000369049.8:c.487G>C
|
ENSP00000358045.4:p.Asp163His
|
|
ENST00000470432.5:n.1505G>C
|
|
|
ENST00000498579.5:n.693G>C
|
|
|
NM_001202858.1:c.487G>C
|
NP_001189787.1:p.Asp163His
|
|
NM_004425.3:c.406G>C
|
NP_004416.2:p.Asp136His
|
|
NM_022664.2:c.406G>C
|
NP_073155.2:p.Asp136His
|
|
NM_004425.4:c.406G>C
MANE Select
|
NP_004416.2:p.Asp136His
|
|
NM_001202858.2:c.487G>C
|
NP_001189787.1:p.Asp163His
|
|
NM_022664.3:c.406G>C
|
NP_073155.2:p.Asp136His
|
|