ENST00000333213.11:c.919G=
MANE Select
|
ENSP00000327487.6:p.Ala307=
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|
ENST00000434205.8:c.616G=
|
ENSP00000406559.4:p.Ala206=
|
|
ENST00000545228.3:c.919G=
|
ENSP00000438169.3:p.Ala307=
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|
ENST00000579449.2:n.718G=
|
|
|
ENST00000580013.6:n.1122G=
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|
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ENST00000679370.1:n.1500G=
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|
|
ENST00000679429.1:c.*377G=
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ENSP00000505403.1:n.*377G=
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|
ENST00000679443.1:n.988G=
|
|
|
ENST00000679782.1:c.919G=
|
ENSP00000505995.1:p.Ala307=
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|
ENST00000679919.1:n.988G=
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|
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ENST00000679928.1:c.*530G=
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ENSP00000506071.1:n.*530G=
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|
ENST00000680528.1:n.944G=
|
|
|
ENST00000680999.1:c.919G=
|
ENSP00000504984.1:p.Ala307=
|
|
ENST00000681282.1:c.*165G=
|
ENSP00000506339.1:n.*165G=
|
|
ENST00000333213.10:c.919G=
|
ENSP00000327487.6:p.Ala307=
|
|
ENST00000545228.2:c.8G=
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|
|
ENST00000578415.1:c.879G=
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|
|
ENST00000583173.5:c.459-7G=
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ENSP00000463619.1:n.459-7G=
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|
NM_207346.2:c.919G=
|
NP_997229.2:p.Ala307=
|
|
XM_005257229.2:c.919G=
|
XP_005257286.1:p.Ala307=
|
|
XM_006721821.2:c.616G=
|
XP_006721884.1:p.Ala206=
|
|
XM_011524616.1:c.919G=
|
XP_011522918.1:p.Ala307=
|
|
XM_011524617.1:c.919G=
|
XP_011522919.1:p.Ala307=
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|
XM_011524618.1:c.919G=
|
XP_011522920.1:p.Ala307=
|
|
XR_243646.2:n.949G=
|
|
|
XM_005257229.4:c.919G=
|
XP_005257286.1:p.Ala307=
|
|
XR_243646.4:n.955G=
|
|
|
NM_207346.3:c.919G=
MANE Select
|
NP_997229.2:p.Ala307=
|
|