ENST00000295897.9:c.1478T>A
MANE Select
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ENSP00000295897.4:p.Val493Glu
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ENST00000295897.8:c.1478T>A
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ENSP00000295897.4:p.Val493Glu
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ENST00000401494.7:c.1133T>A
|
ENSP00000384695.3:p.Val378Glu
|
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ENST00000415165.6:c.902T>A
|
ENSP00000401820.2:p.Val301Glu
|
|
ENST00000476441.6:c.*757T>A
|
ENSP00000423727.1:n.*757T>A
|
|
ENST00000486939.1:n.132T>A
|
|
|
ENST00000503124.5:c.1028T>A
|
ENSP00000421027.1:p.Val343Glu
|
|
ENST00000505649.5:n.1025T>A
|
|
|
ENST00000509063.5:c.1478T>A
|
ENSP00000422784.1:p.Val493Glu
|
|
ENST00000511370.1:c.1011T>A
|
|
|
ENST00000621085.4:c.839T>A
|
ENSP00000483421.1:p.Val280Glu
|
|
ENST00000621628.4:c.839T>A
|
ENSP00000480485.1:p.Val280Glu
|
|
NM_000477.5:c.1478T>A
|
NP_000468.1:p.Val493Glu
|
|
NM_000477.6:c.1478T>A
|
NP_000468.1:p.Val493Glu
|
|
NM_000477.7:c.1478T>A
MANE Select
|
NP_000468.1:p.Val493Glu
|
|