ENST00000309755.9:c.1071C>T
MANE Select
|
ENSP00000312397.4:p.Gly357=
|
|
ENST00000309755.8:c.1071C>T
|
ENSP00000312397.4:p.Gly357=
|
|
ENST00000502381.1:n.658C>T
|
|
|
ENST00000504208.5:c.*335-10664C>T
|
ENSP00000423585.1:n.*335-10664C>T
|
|
ENST00000505853.1:c.951C>T
|
ENSP00000426173.1:p.Gly317=
|
|
ENST00000506491.5:c.825C>T
|
ENSP00000424828.1:p.Gly275=
|
|
ENST00000506873.5:n.696C>T
|
|
|
ENST00000508657.5:c.975C>T
|
ENSP00000422099.1:p.Gly325=
|
|
NM_001257194.1:c.975C>T
|
NP_001244123.1:p.Gly325=
|
|
NM_001257195.1:c.825C>T
|
NP_001244124.1:p.Gly275=
|
|
NM_017415.2:c.1071C>T
|
NP_059111.2:p.Gly357=
|
|
NM_017415.3:c.1071C>T
MANE Select
|
NP_059111.2:p.Gly357=
|
|
NM_001257195.2:c.825C>T
|
NP_001244124.1:p.Gly275=
|
|