ENST00000295897.9:c.1110G=
MANE Select
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ENSP00000295897.4:p.Leu370=
|
|
ENST00000295897.8:c.1110G=
|
ENSP00000295897.4:p.Leu370=
|
|
ENST00000401494.7:c.765G=
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ENSP00000384695.3:p.Leu255=
|
|
ENST00000415165.6:c.534G=
|
ENSP00000401820.2:p.Leu178=
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ENST00000476441.6:c.*389G=
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ENSP00000423727.1:n.*389G=
|
|
ENST00000484992.1:n.430G=
|
|
|
ENST00000503124.5:c.660G=
|
ENSP00000421027.1:p.Leu220=
|
|
ENST00000504043.1:n.113G=
|
|
|
ENST00000505649.5:n.796G=
|
|
|
ENST00000509063.5:c.1110G=
|
ENSP00000422784.1:p.Leu370=
|
|
ENST00000511370.1:c.643G=
|
|
|
ENST00000621085.4:c.491-20G=
|
ENSP00000483421.1:n.491-20G=
|
|
ENST00000621628.4:c.487-16G=
|
ENSP00000480485.1:n.487-16G=
|
|
NM_000477.5:c.1110G=
|
NP_000468.1:p.Leu370=
|
|
NM_000477.6:c.1110G=
|
NP_000468.1:p.Leu370=
|
|
NM_000477.7:c.1110G=
MANE Select
|
NP_000468.1:p.Leu370=
|
|