ENST00000298229.7:c.878C>T
MANE Select
|
ENSP00000298229.2:p.Ala293Val
|
|
ENST00000298229.6:c.878C>T
|
ENSP00000298229.2:p.Ala293Val
|
|
ENST00000538751.5:c.152C>T
|
ENSP00000444619.1:p.Ala51Val
|
|
ENST00000540329.5:c.62C>T
|
ENSP00000440018.1:p.Ala21Val
|
|
ENST00000541756.5:c.680C>T
|
ENSP00000446360.2:p.Ala227Val
|
|
NM_001567.3:c.878C>T
|
NP_001558.3:p.Ala293Val
|
|
XM_005273978.3:c.944C>T
|
XP_005274035.1:p.Ala315Val
|
|
XM_005273979.3:c.944C>T
|
XP_005274036.1:p.Ala315Val
|
|
XM_011544999.1:c.878C>T
|
XP_011543301.1:p.Ala293Val
|
|
XM_011545000.1:c.944C>T
|
XP_011543302.1:p.Ala315Val
|
|
XM_005273979.4:c.944C>T
|
XP_005274036.1:p.Ala315Val
|
|
XM_011544999.2:c.878C>T
|
XP_011543301.1:p.Ala293Val
|
|
XM_024448501.1:c.944C>T
|
XP_024304269.1:p.Ala315Val
|
|
XM_024448502.1:c.944C>T
|
XP_024304270.1:p.Ala315Val
|
|
XM_024448503.1:c.914C>T
|
XP_024304271.1:p.Ala305Val
|
|
XM_024448504.1:c.878C>T
|
XP_024304272.1:p.Ala293Val
|
|
XM_024448505.1:c.944C>T
|
XP_024304273.1:p.Ala315Val
|
|
NM_001567.4:c.878C>T
MANE Select
|
NP_001558.3:p.Ala293Val
|
|