ENST00000367324.8:c.942G>T
MANE Select
|
ENSP00000356293.4:p.Leu314=
|
|
ENST00000263946.7:c.942G>T
|
ENSP00000263946.3:p.Leu314=
|
|
ENST00000352845.3:c.942G>T
|
ENSP00000295597.3:p.Leu314=
|
|
ENST00000367324.7:c.942G>T
|
ENSP00000356293.3:p.Leu314=
|
|
ENST00000475988.1:n.284G>T
|
|
|
ENST00000622031.4:c.939G>T
|
ENSP00000482213.1:p.Leu313=
|
|
NM_000299.3:c.942G>T
|
NP_000290.2:p.Leu314=
|
|
NM_001005337.2:c.942G>T
|
NP_001005337.1:p.Leu314=
|
|
NM_001005337.3:c.942G>T
MANE Select
|
NP_001005337.1:p.Leu314=
|
|
NM_000299.4:c.942G>T
|
NP_000290.2:p.Leu314=
|
|