ENST00000322776.11:c.1003G=
MANE Select
|
ENSP00000322450.6:p.Val335=
|
|
ENST00000647561.1:c.1003G=
|
ENSP00000497587.1:p.Val335=
|
|
ENST00000322776.10:c.1003G=
|
ENSP00000322450.6:p.Val335=
|
|
ENST00000415352.6:c.982G=
|
ENSP00000395368.2:p.Val328=
|
|
ENST00000526169.1:n.656-30G=
|
|
|
ENST00000526770.5:n.1286G=
|
|
|
ENST00000527355.5:c.292G=
|
ENSP00000432637.1:p.Val98=
|
|
ENST00000527923.1:n.345G=
|
|
|
ENST00000529927.5:c.976G=
|
ENSP00000436766.1:p.Val326=
|
|
ENST00000532303.5:c.700G=
|
ENSP00000432015.1:p.Val234=
|
|
ENST00000533919.5:c.407G=
|
ENSP00000435199.1:n.407G=
|
|
NM_001166102.1:c.976G=
|
NP_001159574.1:p.Val326=
|
|
NM_007103.3:c.1003G=
|
NP_009034.2:p.Val335=
|
|
NM_001166102.2:c.976G=
|
NP_001159574.1:p.Val326=
|
|
NM_007103.4:c.1003G=
MANE Select
|
NP_009034.2:p.Val335=
|
|