ENST00000322344.8:c.1436T>A
MANE Select
|
ENSP00000323511.2:p.Met479Lys
|
|
ENST00000636840.1:c.59+147T>A
|
|
|
ENST00000640501.1:c.42T>A
|
|
|
ENST00000322344.7:c.1436T>A
|
ENSP00000323511.2:p.Met479Lys
|
|
ENST00000593946.5:c.*1363T>A
|
ENSP00000468896.1:n.*1363T>A
|
|
ENST00000594661.5:n.1937T>A
|
|
|
ENST00000595081.5:n.339T>A
|
|
|
ENST00000596014.5:c.1436T>A
|
ENSP00000472300.1:p.Met479Lys
|
|
ENST00000597965.2:c.143T>A
|
ENSP00000471097.2:p.Met48Lys
|
|
ENST00000599454.5:n.356T>A
|
|
|
ENST00000600573.5:c.1343T>A
|
ENSP00000469826.1:p.Met448Lys
|
|
ENST00000600910.5:c.1326T>A
|
ENSP00000473137.1:p.His442Gln
|
|
ENST00000601816.3:n.508T>A
|
|
|
ENST00000625216.2:c.517T>A
|
ENSP00000486898.1:n.517T>A
|
|
ENST00000627232.2:c.1356T>A
|
ENSP00000486037.1:n.1356T>A
|
|
ENST00000631020.2:c.1328T>A
|
ENSP00000486707.1:p.Met443Lys
|
|
NM_007254.3:c.1436T>A
|
NP_009185.2:p.Met479Lys
|
|
NM_007254.4:c.1436T>A
MANE Select
|
NP_009185.2:p.Met479Lys
|
|