ENST00000367324.8:c.984G>C
MANE Select
|
ENSP00000356293.4:p.Gln328His
|
|
ENST00000263946.7:c.984G>C
|
ENSP00000263946.3:p.Gln328His
|
|
ENST00000352845.3:c.984G>C
|
ENSP00000295597.3:p.Gln328His
|
|
ENST00000367324.7:c.984G>C
|
ENSP00000356293.3:p.Gln328His
|
|
ENST00000475988.1:n.326G>C
|
|
|
ENST00000622031.4:c.981G>C
|
ENSP00000482213.1:p.Gln327His
|
|
NM_000299.3:c.984G>C
|
NP_000290.2:p.Gln328His
|
|
NM_001005337.2:c.984G>C
|
NP_001005337.1:p.Gln328His
|
|
NM_001005337.3:c.984G>C
MANE Select
|
NP_001005337.1:p.Gln328His
|
|
NM_000299.4:c.984G>C
|
NP_000290.2:p.Gln328His
|
|