ENST00000295897.9:c.1598T>C
MANE Select
|
ENSP00000295897.4:p.Phe533Ser
|
|
ENST00000295897.8:c.1598T>C
|
ENSP00000295897.4:p.Phe533Ser
|
|
ENST00000401494.7:c.1253T>C
|
ENSP00000384695.3:p.Phe418Ser
|
|
ENST00000415165.6:c.1022T>C
|
ENSP00000401820.2:p.Phe341Ser
|
|
ENST00000476441.6:c.*877T>C
|
ENSP00000423727.1:n.*877T>C
|
|
ENST00000486939.1:n.252T>C
|
|
|
ENST00000503124.5:c.1148T>C
|
ENSP00000421027.1:p.Phe383Ser
|
|
ENST00000505649.5:n.1145T>C
|
|
|
ENST00000509063.5:c.1598T>C
|
ENSP00000422784.1:p.Phe533Ser
|
|
ENST00000511370.1:c.1131T>C
|
|
|
ENST00000621085.4:c.959T>C
|
ENSP00000483421.1:p.Phe320Ser
|
|
ENST00000621628.4:c.959T>C
|
ENSP00000480485.1:p.Phe320Ser
|
|
NM_000477.5:c.1598T>C
|
NP_000468.1:p.Phe533Ser
|
|
NM_000477.6:c.1598T>C
|
NP_000468.1:p.Phe533Ser
|
|
NM_000477.7:c.1598T>C
MANE Select
|
NP_000468.1:p.Phe533Ser
|
|