ENST00000333213.11:c.*141A>G
MANE Select
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ENSP00000327487.6:n.*141A>G
|
|
ENST00000434205.8:c.*141A>G
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ENSP00000406559.4:n.*141A>G
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ENST00000545228.3:c.*221A>G
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ENSP00000438169.3:n.*221A>G
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ENST00000577197.2:n.920A>G
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|
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ENST00000579449.2:n.2462A>G
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|
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ENST00000580013.6:n.2866A>G
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|
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ENST00000679370.1:n.3244A>G
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ENST00000679429.1:c.*1180A>G
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ENSP00000505403.1:n.*1180A>G
|
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ENST00000679443.1:n.1791A>G
|
|
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ENST00000679782.1:c.*421A>G
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ENSP00000505995.1:n.*421A>G
|
|
ENST00000679919.1:n.1993A>G
|
|
|
ENST00000679928.1:c.*2274A>G
|
ENSP00000506071.1:n.*2274A>G
|
|
ENST00000680999.1:c.*141A>G
|
ENSP00000504984.1:n.*141A>G
|
|
ENST00000681282.1:c.*1909A>G
|
ENSP00000506339.1:n.*1909A>G
|
|
ENST00000333213.10:c.*141A>G
|
ENSP00000327487.6:n.*141A>G
|
|
ENST00000545228.2:c.999A>G
|
|
|
ENST00000577197.1:n.470A>G
|
|
|
NM_207346.2:c.*141A>G
|
NP_997229.2:n.*141A>G
|
|
XM_005257229.2:c.*221A>G
|
XP_005257286.1:n.*221A>G
|
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XM_006721821.2:c.*221A>G
|
XP_006721884.1:n.*221A>G
|
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XM_011524616.1:c.*221A>G
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XP_011522918.1:n.*221A>G
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XM_011524618.1:c.*141A>G
|
XP_011522920.1:n.*141A>G
|
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XR_243646.2:n.1954A>G
|
|
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XM_005257229.4:c.*221A>G
|
XP_005257286.1:n.*221A>G
|
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XR_243646.4:n.1960A>G
|
|
|
NM_207346.3:c.*141A>G
MANE Select
|
NP_997229.2:n.*141A>G
|
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