ENST00000309755.9:c.1189T>C
MANE Select
|
ENSP00000312397.4:p.Tyr397His
|
|
ENST00000309755.8:c.1189T>C
|
ENSP00000312397.4:p.Tyr397His
|
|
ENST00000502381.1:n.776T>C
|
|
|
ENST00000504208.5:c.*335-10546T>C
|
ENSP00000423585.1:n.*335-10546T>C
|
|
ENST00000505853.1:c.1069T>C
|
ENSP00000426173.1:p.Tyr357His
|
|
ENST00000506491.5:c.943T>C
|
ENSP00000424828.1:p.Tyr315His
|
|
ENST00000506873.5:n.814T>C
|
|
|
ENST00000508657.5:c.1093T>C
|
ENSP00000422099.1:p.Tyr365His
|
|
NM_001257194.1:c.1093T>C
|
NP_001244123.1:p.Tyr365His
|
|
NM_001257195.1:c.943T>C
|
NP_001244124.1:p.Tyr315His
|
|
NM_017415.2:c.1189T>C
|
NP_059111.2:p.Tyr397His
|
|
NM_017415.3:c.1189T>C
MANE Select
|
NP_059111.2:p.Tyr397His
|
|
NM_001257195.2:c.943T>C
|
NP_001244124.1:p.Tyr315His
|
|