ENST00000309755.9:c.1085G>A
MANE Select
|
ENSP00000312397.4:p.Arg362Gln
|
|
ENST00000309755.8:c.1085G>A
|
ENSP00000312397.4:p.Arg362Gln
|
|
ENST00000502381.1:n.672G>A
|
|
|
ENST00000504208.5:c.*335-10650G>A
|
ENSP00000423585.1:n.*335-10650G>A
|
|
ENST00000505853.1:c.965G>A
|
ENSP00000426173.1:p.Arg322Gln
|
|
ENST00000506491.5:c.839G>A
|
ENSP00000424828.1:p.Arg280Gln
|
|
ENST00000506873.5:n.710G>A
|
|
|
ENST00000508657.5:c.989G>A
|
ENSP00000422099.1:p.Arg330Gln
|
|
NM_001257194.1:c.989G>A
|
NP_001244123.1:p.Arg330Gln
|
|
NM_001257195.1:c.839G>A
|
NP_001244124.1:p.Arg280Gln
|
|
NM_017415.2:c.1085G>A
|
NP_059111.2:p.Arg362Gln
|
|
NM_017415.3:c.1085G>A
MANE Select
|
NP_059111.2:p.Arg362Gln
|
|
NM_001257195.2:c.839G>A
|
NP_001244124.1:p.Arg280Gln
|
|