ENST00000697953.1:n.200A>T
|
|
|
ENST00000698016.1:c.171A>T
|
ENSP00000513502.1:p.Arg57=
|
|
ENST00000698022.1:c.129A>T
|
ENSP00000513504.1:p.Arg43=
|
|
ENST00000698027.1:c.171A>T
|
ENSP00000513505.1:p.Arg57=
|
|
ENST00000448276.7:c.312A>T
MANE Select
|
ENSP00000392617.2:p.Arg104=
|
|
ENST00000225742.13:c.87A>T
|
ENSP00000225742.9:p.Arg29=
|
|
ENST00000323347.14:c.168A>T
|
ENSP00000318451.10:p.Arg56=
|
|
ENST00000448276.6:c.312A>T
|
ENSP00000392617.2:p.Arg104=
|
|
ENST00000577686.1:n.53-293A>T
|
|
|
ENST00000580054.1:c.96A>T
|
ENSP00000463793.1:p.Arg32=
|
|
ENST00000584400.5:c.217-293A>T
|
ENSP00000464503.1:n.217-293A>T
|
|
ENST00000613943.4:c.201A>T
|
ENSP00000483605.1:p.Arg67=
|
|
NM_001098426.1:c.312A>T
|
NP_001091896.1:p.Arg104=
|
|
XM_005257604.2:c.87A>T
|
XP_005257661.2:p.Arg29=
|
|
NM_001330439.1:c.87A>T
|
NP_001317368.1:p.Arg29=
|
|
NM_001330440.1:c.168A>T
|
NP_001317369.1:p.Arg56=
|
|
NM_001098426.2:c.312A>T
MANE Select
|
NP_001091896.1:p.Arg104=
|
|
NM_001330440.2:c.168A>T
|
NP_001317369.1:p.Arg56=
|
|