ENST00000295897.9:c.1554T>C
MANE Select
|
ENSP00000295897.4:p.Asp518=
|
|
ENST00000295897.8:c.1554T>C
|
ENSP00000295897.4:p.Asp518=
|
|
ENST00000401494.7:c.1209T>C
|
ENSP00000384695.3:p.Asp403=
|
|
ENST00000415165.6:c.978T>C
|
ENSP00000401820.2:p.Asp326=
|
|
ENST00000476441.6:c.*833T>C
|
ENSP00000423727.1:n.*833T>C
|
|
ENST00000486939.1:n.208T>C
|
|
|
ENST00000503124.5:c.1104T>C
|
ENSP00000421027.1:p.Asp368=
|
|
ENST00000505649.5:n.1101T>C
|
|
|
ENST00000509063.5:c.1554T>C
|
ENSP00000422784.1:p.Asp518=
|
|
ENST00000511370.1:c.1087T>C
|
|
|
ENST00000621085.4:c.915T>C
|
ENSP00000483421.1:p.Asp305=
|
|
ENST00000621628.4:c.915T>C
|
ENSP00000480485.1:p.Asp305=
|
|
NM_000477.5:c.1554T>C
|
NP_000468.1:p.Asp518=
|
|
NM_000477.6:c.1554T>C
|
NP_000468.1:p.Asp518=
|
|
NM_000477.7:c.1554T>C
MANE Select
|
NP_000468.1:p.Asp518=
|
|