ENST00000388958.8:c.1182T>C
|
ENSP00000373610.3:p.Val394=
|
|
ENST00000646100.2:c.1182T>C
MANE Select
|
ENSP00000496564.2:p.Val394=
|
|
ENST00000647277.1:c.1058T>C
|
ENSP00000495594.1:p.Leu353Ser
|
|
ENST00000286149.8:c.1224T>C
|
ENSP00000286149.4:p.Val408=
|
|
ENST00000388956.8:c.945T>C
|
ENSP00000373608.4:p.Val315=
|
|
ENST00000388957.3:c.210T>C
|
ENSP00000373609.3:p.Val70=
|
|
ENST00000388958.7:c.1182T>C
|
ENSP00000373610.3:p.Val394=
|
|
ENST00000563871.5:n.402T>C
|
|
|
NM_001161683.1:c.945T>C
|
NP_001155155.1:p.Val315=
|
|
NM_144672.3:c.1182T>C
|
NP_653273.3:p.Val394=
|
|
NM_170664.2:c.210T>C
|
NP_733764.1:p.Val70=
|
|
XM_011545747.1:c.1182T>C
|
XP_011544049.1:p.Val394=
|
|
XM_011545748.1:c.51T>C
|
XP_011544050.1:p.Val17=
|
|
NM_144672.4:c.1182T>C
MANE Select
|
NP_653273.3:p.Val394=
|
|
XM_011545748.2:c.51T>C
|
XP_011544050.2:p.Val17=
|
|
XR_002957775.1:n.277T>C
|
|
|
NM_001161683.2:c.945T>C
|
NP_001155155.1:p.Val315=
|
|
NM_170664.3:c.210T>C
|
NP_733764.1:p.Val70=
|
|