ENST00000295897.9:c.1151G>T
MANE Select
|
ENSP00000295897.4:p.Cys384Phe
|
|
ENST00000295897.8:c.1151G>T
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ENSP00000295897.4:p.Cys384Phe
|
|
ENST00000401494.7:c.806G>T
|
ENSP00000384695.3:p.Cys269Phe
|
|
ENST00000415165.6:c.575G>T
|
ENSP00000401820.2:p.Cys192Phe
|
|
ENST00000476441.6:c.*430G>T
|
ENSP00000423727.1:n.*430G>T
|
|
ENST00000484992.1:n.471G>T
|
|
|
ENST00000503124.5:c.701G>T
|
ENSP00000421027.1:p.Cys234Phe
|
|
ENST00000504043.1:n.154G>T
|
|
|
ENST00000505649.5:n.837G>T
|
|
|
ENST00000509063.5:c.1151G>T
|
ENSP00000422784.1:p.Cys384Phe
|
|
ENST00000511370.1:c.684G>T
|
|
|
ENST00000621085.4:c.512G>T
|
ENSP00000483421.1:p.Cys171Phe
|
|
ENST00000621628.4:c.512G>T
|
ENSP00000480485.1:p.Cys171Phe
|
|
NM_000477.5:c.1151G>T
|
NP_000468.1:p.Cys384Phe
|
|
NM_000477.6:c.1151G>T
|
NP_000468.1:p.Cys384Phe
|
|
NM_000477.7:c.1151G>T
MANE Select
|
NP_000468.1:p.Cys384Phe
|
|