ENST00000322344.8:c.1303G>T
MANE Select
|
ENSP00000323511.2:p.Val435Phe
|
|
ENST00000322344.7:c.1303G>T
|
ENSP00000323511.2:p.Val435Phe
|
|
ENST00000593946.5:c.*1230G>T
|
ENSP00000468896.1:n.*1230G>T
|
|
ENST00000594661.5:n.1804G>T
|
|
|
ENST00000595081.5:n.206G>T
|
|
|
ENST00000596014.5:c.1303G>T
|
ENSP00000472300.1:p.Val435Phe
|
|
ENST00000597965.2:c.10G>T
|
ENSP00000471097.2:p.Val4Phe
|
|
ENST00000599454.5:n.223G>T
|
|
|
ENST00000600573.5:c.1210G>T
|
ENSP00000469826.1:p.Val404Phe
|
|
ENST00000600910.5:c.1193G>T
|
ENSP00000473137.1:p.Arg398Leu
|
|
ENST00000601816.3:n.278G>T
|
|
|
ENST00000625216.2:c.384G>T
|
ENSP00000486898.1:n.384G>T
|
|
ENST00000627232.2:c.1223G>T
|
ENSP00000486037.1:n.1223G>T
|
|
ENST00000631020.2:c.1195G>T
|
ENSP00000486707.1:p.Val399Phe
|
|
NM_007254.3:c.1303G>T
|
NP_009185.2:p.Val435Phe
|
|
NM_007254.4:c.1303G>T
MANE Select
|
NP_009185.2:p.Val435Phe
|
|