ENST00000322776.11:c.951G>C
MANE Select
|
ENSP00000322450.6:p.Val317=
|
|
ENST00000647561.1:c.951G>C
|
ENSP00000497587.1:p.Val317=
|
|
ENST00000322776.10:c.951G>C
|
ENSP00000322450.6:p.Val317=
|
|
ENST00000415352.6:c.930G>C
|
ENSP00000395368.2:p.Val310=
|
|
ENST00000526169.1:n.656-82G>C
|
|
|
ENST00000526770.5:n.1234G>C
|
|
|
ENST00000527355.5:c.240G>C
|
ENSP00000432637.1:p.Val80=
|
|
ENST00000527923.1:n.293G>C
|
|
|
ENST00000529927.5:c.924G>C
|
ENSP00000436766.1:p.Val308=
|
|
ENST00000532303.5:c.648G>C
|
ENSP00000432015.1:p.Val216=
|
|
ENST00000533919.5:c.392-37G>C
|
ENSP00000435199.1:n.392-37G>C
|
|
NM_001166102.1:c.924G>C
|
NP_001159574.1:p.Val308=
|
|
NM_007103.3:c.951G>C
|
NP_009034.2:p.Val317=
|
|
NM_001166102.2:c.924G>C
|
NP_001159574.1:p.Val308=
|
|
NM_007103.4:c.951G>C
MANE Select
|
NP_009034.2:p.Val317=
|
|