ENST00000309755.9:c.1082T>G
MANE Select
|
ENSP00000312397.4:p.Val361Gly
|
|
ENST00000309755.8:c.1082T>G
|
ENSP00000312397.4:p.Val361Gly
|
|
ENST00000502381.1:n.669T>G
|
|
|
ENST00000504208.5:c.*335-10653T>G
|
ENSP00000423585.1:n.*335-10653T>G
|
|
ENST00000505853.1:c.962T>G
|
ENSP00000426173.1:p.Val321Gly
|
|
ENST00000506491.5:c.836T>G
|
ENSP00000424828.1:p.Val279Gly
|
|
ENST00000506873.5:n.707T>G
|
|
|
ENST00000508657.5:c.986T>G
|
ENSP00000422099.1:p.Val329Gly
|
|
NM_001257194.1:c.986T>G
|
NP_001244123.1:p.Val329Gly
|
|
NM_001257195.1:c.836T>G
|
NP_001244124.1:p.Val279Gly
|
|
NM_017415.2:c.1082T>G
|
NP_059111.2:p.Val361Gly
|
|
NM_017415.3:c.1082T>G
MANE Select
|
NP_059111.2:p.Val361Gly
|
|
NM_001257195.2:c.836T>G
|
NP_001244124.1:p.Val279Gly
|
|