ENST00000636937.2:c.2584G=
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ENSP00000516154.1:p.Ala862=
|
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ENST00000268124.11:c.2584G=
MANE Select
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ENSP00000268124.5:p.Ala862=
|
|
ENST00000530292.3:c.2185G=
|
ENSP00000432885.2:p.Ala729=
|
|
ENST00000635986.2:c.2584G=
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ENSP00000490653.2:p.Ala862=
|
|
ENST00000636774.1:c.*1151G=
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ENSP00000489799.1:n.*1151G=
|
|
ENST00000637238.1:c.1281G=
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ENSP00000490756.1:n.1281G=
|
|
ENST00000637264.1:c.1656G=
|
|
|
ENST00000666746.1:c.2161G=
|
|
|
ENST00000670281.1:c.800+212G=
|
ENSP00000499709.1:n.800+212G=
|
|
ENST00000672071.1:n.2782G=
|
|
|
ENST00000672923.2:n.2526G=
|
|
|
ENST00000268124.9:c.2584G=
|
ENSP00000268124.5:p.Ala862=
|
|
ENST00000442287.6:c.2584G=
|
ENSP00000399851.2:p.Ala862=
|
|
ENST00000528881.2:c.196-490G=
|
|
|
ENST00000530715.5:c.186-881G=
|
ENSP00000431395.1:n.186-881G=
|
|
ENST00000631044.2:c.*2008G=
|
ENSP00000486730.1:n.*2008G=
|
|
NM_001126131.1:c.2584G=
|
NP_001119603.1:p.Ala862=
|
|
NM_002693.2:c.2584G=
|
NP_002684.1:p.Ala862=
|
|
NM_001126131.2:c.2584G=
|
NP_001119603.1:p.Ala862=
|
|
NM_002693.3:c.2584G=
MANE Select
|
NP_002684.1:p.Ala862=
|
|