ENST00000322344.8:c.1437G>A
MANE Select
|
ENSP00000323511.2:p.Met479Ile
|
|
ENST00000636840.1:c.59+148G>A
|
|
|
ENST00000640501.1:c.43G>A
|
|
|
ENST00000322344.7:c.1437G>A
|
ENSP00000323511.2:p.Met479Ile
|
|
ENST00000593946.5:c.*1364G>A
|
ENSP00000468896.1:n.*1364G>A
|
|
ENST00000594661.5:n.1938G>A
|
|
|
ENST00000595081.5:n.340G>A
|
|
|
ENST00000596014.5:c.1437G>A
|
ENSP00000472300.1:p.Met479Ile
|
|
ENST00000597965.2:c.144G>A
|
ENSP00000471097.2:p.Met48Ile
|
|
ENST00000599454.5:n.357G>A
|
|
|
ENST00000600573.5:c.1344G>A
|
ENSP00000469826.1:p.Met448Ile
|
|
ENST00000600910.5:c.1327G>A
|
ENSP00000473137.1:p.Val443Ile
|
|
ENST00000601816.3:n.509G>A
|
|
|
ENST00000625216.2:c.518G>A
|
ENSP00000486898.1:n.518G>A
|
|
ENST00000627232.2:c.1357G>A
|
ENSP00000486037.1:n.1357G>A
|
|
ENST00000631020.2:c.1329G>A
|
ENSP00000486707.1:p.Met443Ile
|
|
NM_007254.3:c.1437G>A
|
NP_009185.2:p.Met479Ile
|
|
NM_007254.4:c.1437G>A
MANE Select
|
NP_009185.2:p.Met479Ile
|
|