ENST00000312465.12:c.713A>C
MANE Select
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ENSP00000311697.7:p.Lys238Thr
|
|
ENST00000312465.11:c.713A>C
|
ENSP00000311697.7:p.Lys238Thr
|
|
ENST00000456523.3:c.*237A>C
|
ENSP00000398353.3:n.*237A>C
|
|
ENST00000503413.1:n.662A>C
|
|
|
ENST00000507780.1:c.342+11566A>C
|
ENSP00000423903.1:n.342+11566A>C
|
|
NM_001291812.1:c.284A>C
|
NP_001278741.1:p.Lys95Thr
|
|
NM_004464.3:c.713A>C
|
NP_004455.2:p.Lys238Thr
|
|
NM_033143.2:c.*237A>C
|
NP_149134.1:n.*237A>C
|
|
NM_001291812.2:c.284A>C
|
NP_001278741.1:p.Lys95Thr
|
|
NM_004464.4:c.713A>C
MANE Select
|
NP_004455.2:p.Lys238Thr
|
|