ENST00000322776.11:c.1027G=
MANE Select
|
ENSP00000322450.6:p.Val343=
|
|
ENST00000647561.1:c.1027G=
|
ENSP00000497587.1:p.Val343=
|
|
ENST00000322776.10:c.1027G=
|
ENSP00000322450.6:p.Val343=
|
|
ENST00000415352.6:c.1006G=
|
ENSP00000395368.2:p.Val336=
|
|
ENST00000526169.1:n.656-6G=
|
|
|
ENST00000526770.5:n.1310G=
|
|
|
ENST00000527355.5:c.316G=
|
ENSP00000432637.1:p.Val106=
|
|
ENST00000527923.1:n.369G=
|
|
|
ENST00000529927.5:c.1000G=
|
ENSP00000436766.1:p.Val334=
|
|
ENST00000532303.5:c.724G=
|
ENSP00000432015.1:p.Val242=
|
|
ENST00000533919.5:c.431G=
|
ENSP00000435199.1:n.431G=
|
|
NM_001166102.1:c.1000G=
|
NP_001159574.1:p.Val334=
|
|
NM_007103.3:c.1027G=
|
NP_009034.2:p.Val343=
|
|
NM_001166102.2:c.1000G=
|
NP_001159574.1:p.Val334=
|
|
NM_007103.4:c.1027G=
MANE Select
|
NP_009034.2:p.Val343=
|
|