ENST00000295897.9:c.1606G>T
MANE Select
|
ENSP00000295897.4:p.Asp536Tyr
|
|
ENST00000295897.8:c.1606G>T
|
ENSP00000295897.4:p.Asp536Tyr
|
|
ENST00000401494.7:c.1261G>T
|
ENSP00000384695.3:p.Asp421Tyr
|
|
ENST00000415165.6:c.1030G>T
|
ENSP00000401820.2:p.Asp344Tyr
|
|
ENST00000476441.6:c.*885G>T
|
ENSP00000423727.1:n.*885G>T
|
|
ENST00000486939.1:n.260G>T
|
|
|
ENST00000503124.5:c.1156G>T
|
ENSP00000421027.1:p.Asp386Tyr
|
|
ENST00000505649.5:n.1153G>T
|
|
|
ENST00000509063.5:c.1606G>T
|
ENSP00000422784.1:p.Asp536Tyr
|
|
ENST00000511370.1:c.1139G>T
|
|
|
ENST00000621085.4:c.967G>T
|
ENSP00000483421.1:p.Asp323Tyr
|
|
ENST00000621628.4:c.967G>T
|
ENSP00000480485.1:p.Asp323Tyr
|
|
NM_000477.5:c.1606G>T
|
NP_000468.1:p.Asp536Tyr
|
|
NM_000477.6:c.1606G>T
|
NP_000468.1:p.Asp536Tyr
|
|
NM_000477.7:c.1606G>T
MANE Select
|
NP_000468.1:p.Asp536Tyr
|
|