ENST00000298229.7:c.904C>A
MANE Select
|
ENSP00000298229.2:p.Arg302Ser
|
|
ENST00000298229.6:c.904C>A
|
ENSP00000298229.2:p.Arg302Ser
|
|
ENST00000538751.5:c.178C>A
|
ENSP00000444619.1:p.Arg60Ser
|
|
ENST00000540329.5:c.88C>A
|
ENSP00000440018.1:p.Arg30Ser
|
|
ENST00000541756.5:c.706C>A
|
ENSP00000446360.2:p.Arg236Ser
|
|
NM_001567.3:c.904C>A
|
NP_001558.3:p.Arg302Ser
|
|
XM_005273978.3:c.970C>A
|
XP_005274035.1:p.Arg324Ser
|
|
XM_005273979.3:c.970C>A
|
XP_005274036.1:p.Arg324Ser
|
|
XM_011544999.1:c.904C>A
|
XP_011543301.1:p.Arg302Ser
|
|
XM_011545000.1:c.970C>A
|
XP_011543302.1:p.Arg324Ser
|
|
XM_005273979.4:c.970C>A
|
XP_005274036.1:p.Arg324Ser
|
|
XM_011544999.2:c.904C>A
|
XP_011543301.1:p.Arg302Ser
|
|
XM_024448501.1:c.970C>A
|
XP_024304269.1:p.Arg324Ser
|
|
XM_024448502.1:c.970C>A
|
XP_024304270.1:p.Arg324Ser
|
|
XM_024448503.1:c.940C>A
|
XP_024304271.1:p.Arg314Ser
|
|
XM_024448504.1:c.904C>A
|
XP_024304272.1:p.Arg302Ser
|
|
XM_024448505.1:c.970C>A
|
XP_024304273.1:p.Arg324Ser
|
|
NM_001567.4:c.904C>A
MANE Select
|
NP_001558.3:p.Arg302Ser
|
|