ENST00000355280.11:c.*419G>C
MANE Select
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ENSP00000347427.6:n.*419G>C
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ENST00000347992.11:c.*419G>C
|
ENSP00000269296.7:n.*419G>C
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ENST00000355280.10:c.*419G>C
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ENSP00000347427.6:n.*419G>C
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ENST00000571207.5:c.4214G>C
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|
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ENST00000572330.5:n.5200G>C
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|
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ENST00000574453.5:c.*4087G>C
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ENSP00000461500.1:n.*4087G>C
|
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ENST00000574871.1:n.2796G>C
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|
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NM_001024937.3:c.*419G>C
|
NP_001020108.1:n.*419G>C
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|
NM_015716.4:c.*419G>C
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NP_056531.1:n.*419G>C
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|
NM_153827.4:c.*419G>C
|
NP_722549.2:n.*419G>C
|
|
NM_170663.4:c.*419G>C
|
NP_733763.1:n.*419G>C
|
|
XM_005256664.2:c.*419G>C
|
XP_005256721.1:n.*419G>C
|
|
XM_005256665.2:c.*419G>C
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XP_005256722.1:n.*419G>C
|
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XM_006721530.2:c.*419G>C
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XP_006721593.1:n.*419G>C
|
|
XM_006721531.2:c.*419G>C
|
XP_006721594.1:n.*419G>C
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|
XM_006721532.2:c.*419G>C
|
XP_006721595.1:n.*419G>C
|
|
XM_006721533.2:c.*419G>C
|
XP_006721596.1:n.*419G>C
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XM_006721534.2:c.*419G>C
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XP_006721597.1:n.*419G>C
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XM_006721535.2:c.*419G>C
|
XP_006721598.1:n.*419G>C
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XM_006721536.2:c.*419G>C
|
XP_006721599.1:n.*419G>C
|
|
XM_006721538.2:c.*419G>C
|
XP_006721601.1:n.*419G>C
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XM_011523905.1:c.*419G>C
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XP_011522207.1:n.*419G>C
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XM_011523906.1:c.*419G>C
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XP_011522208.1:n.*419G>C
|
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XM_011523907.1:c.*419G>C
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XP_011522209.1:n.*419G>C
|
|
XM_011523908.1:c.*419G>C
|
XP_011522210.1:n.*419G>C
|
|
NM_001321236.1:c.*419G>C
|
NP_001308165.1:n.*419G>C
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|
XM_017024704.1:c.*419G>C
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XP_016880193.1:n.*419G>C
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|
XM_017024705.1:c.*419G>C
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XP_016880194.1:n.*419G>C
|
|
XM_017024706.1:c.*419G>C
|
XP_016880195.1:n.*419G>C
|
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XM_017024707.2:c.*419G>C
|
XP_016880196.1:n.*419G>C
|
|
XM_017024708.1:c.*419G>C
|
XP_016880197.1:n.*419G>C
|
|
XR_001752522.2:n.4763G>C
|
|
|
NM_153827.5:c.*419G>C
MANE Select
|
NP_722549.2:n.*419G>C
|
|
NM_001024937.4:c.*419G>C
|
NP_001020108.1:n.*419G>C
|
|
NM_001321236.2:c.*419G>C
|
NP_001308165.1:n.*419G>C
|
|
NM_015716.5:c.*419G>C
|
NP_056531.1:n.*419G>C
|
|
NM_170663.5:c.*419G>C
|
NP_733763.1:n.*419G>C
|
|