ENST00000697953.1:n.107A>T
|
|
|
ENST00000698016.1:c.78A>T
|
ENSP00000513502.1:p.Arg26=
|
|
ENST00000698022.1:c.36A>T
|
ENSP00000513504.1:p.Arg12=
|
|
ENST00000698027.1:c.78A>T
|
ENSP00000513505.1:p.Arg26=
|
|
ENST00000448276.7:c.219A>T
MANE Select
|
ENSP00000392617.2:p.Arg73=
|
|
ENST00000225742.13:c.-7A>T
|
ENSP00000225742.9:n.-7A>T
|
|
ENST00000323347.14:c.75A>T
|
ENSP00000318451.10:p.Arg25=
|
|
ENST00000448276.6:c.219A>T
|
ENSP00000392617.2:p.Arg73=
|
|
ENST00000577686.1:n.53-386A>T
|
|
|
ENST00000580054.1:c.3A>T
|
ENSP00000463793.1:p.Arg1=
|
|
ENST00000584400.5:c.217-386A>T
|
ENSP00000464503.1:n.217-386A>T
|
|
ENST00000613943.4:c.108A>T
|
ENSP00000483605.1:p.Arg36=
|
|
NM_001098426.1:c.219A>T
|
NP_001091896.1:p.Arg73=
|
|
XM_005257604.2:c.-7A>T
|
XP_005257661.2:n.-7A>T
|
|
NM_001330439.1:c.-7A>T
|
NP_001317368.1:n.-7A>T
|
|
NM_001330440.1:c.75A>T
|
NP_001317369.1:p.Arg25=
|
|
NM_001098426.2:c.219A>T
MANE Select
|
NP_001091896.1:p.Arg73=
|
|
NM_001330440.2:c.75A>T
|
NP_001317369.1:p.Arg25=
|
|