ENST00000309424.8:c.88T>G
MANE Select
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ENSP00000310966.3:p.Phe30Val
|
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ENST00000309424.7:c.88T>G
|
ENSP00000310966.3:p.Phe30Val
|
|
ENST00000589804.1:c.94T>G
|
ENSP00000465099.1:p.Phe32Val
|
|
ENST00000590794.1:c.20+441T>G
|
|
|
ENST00000592852.1:c.-447T>G
|
ENSP00000467771.1:n.-447T>G
|
|
NM_001297590.1:c.94T>G
|
NP_001284519.1:p.Phe32Val
|
|
NM_012099.1:c.88T>G
|
NP_036231.1:p.Phe30Val
|
|
NM_001297590.2:c.94T>G
|
NP_001284519.1:p.Phe32Val
|
|
NM_012099.2:c.88T>G
|
NP_036231.1:p.Phe30Val
|
|
NM_001297590.3:c.94T>G
|
NP_001284519.1:p.Phe32Val
|
|
NM_012099.3:c.88T>G
MANE Select
|
NP_036231.1:p.Phe30Val
|
|