ENST00000322344.8:c.1444T>A
MANE Select
|
ENSP00000323511.2:p.Tyr482Asn
|
|
ENST00000636840.1:c.59+155T>A
|
|
|
ENST00000640501.1:c.50T>A
|
|
|
ENST00000322344.7:c.1444T>A
|
ENSP00000323511.2:p.Tyr482Asn
|
|
ENST00000593946.5:c.*1371T>A
|
ENSP00000468896.1:n.*1371T>A
|
|
ENST00000594661.5:n.1945T>A
|
|
|
ENST00000595081.5:n.347T>A
|
|
|
ENST00000596014.5:c.1444T>A
|
ENSP00000472300.1:p.Tyr482Asn
|
|
ENST00000597965.2:c.151T>A
|
ENSP00000471097.2:p.Tyr51Asn
|
|
ENST00000599454.5:n.364T>A
|
|
|
ENST00000600573.5:c.1351T>A
|
ENSP00000469826.1:p.Tyr451Asn
|
|
ENST00000600910.5:c.1334T>A
|
ENSP00000473137.1:p.Leu445Gln
|
|
ENST00000601816.3:n.516T>A
|
|
|
ENST00000625216.2:c.525T>A
|
ENSP00000486898.1:n.525T>A
|
|
ENST00000627232.2:c.1364T>A
|
ENSP00000486037.1:n.1364T>A
|
|
ENST00000631020.2:c.1336T>A
|
ENSP00000486707.1:p.Tyr446Asn
|
|
NM_007254.3:c.1444T>A
|
NP_009185.2:p.Tyr482Asn
|
|
NM_007254.4:c.1444T>A
MANE Select
|
NP_009185.2:p.Tyr482Asn
|
|