ENST00000262367.10:c.2158+236A>G
MANE Select
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ENSP00000262367.5:n.2158+236A>G
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ENST00000262367.9:c.2158+236A>G
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ENSP00000262367.5:n.2158+236A>G
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ENST00000382070.7:c.2044+236A>G
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ENSP00000371502.3:n.2044+236A>G
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ENST00000570939.2:c.763+236A>G
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ENSP00000461002.2:n.763+236A>G
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ENST00000571826.5:c.207+236A>G
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|
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ENST00000572134.1:c.426+634A>G
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NM_001079846.1:c.2044+236A>G
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NP_001073315.1:n.2044+236A>G
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NM_004380.2:c.2158+236A>G
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NP_004371.2:n.2158+236A>G
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XM_005255124.3:c.2113+634A>G
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XP_005255181.1:n.2113+634A>G
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XM_005255125.3:c.2158+236A>G
|
XP_005255182.1:n.2158+236A>G
|
|
XM_006720848.2:c.2158+236A>G
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XP_006720911.1:n.2158+236A>G
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|
XM_011522380.1:c.2104+236A>G
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XP_011520682.1:n.2104+236A>G
|
|
XM_011522381.1:c.1405+236A>G
|
XP_011520683.1:n.1405+236A>G
|
|
XM_011522382.1:c.2158+236A>G
|
XP_011520684.1:n.2158+236A>G
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XM_005255124.4:c.2113+634A>G
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XP_005255181.1:n.2113+634A>G
|
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XM_005255125.4:c.2158+236A>G
|
XP_005255182.1:n.2158+236A>G
|
|
XM_006720848.3:c.2158+236A>G
|
XP_006720911.1:n.2158+236A>G
|
|
XM_011522381.2:c.1405+236A>G
|
XP_011520683.1:n.1405+236A>G
|
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XM_011522382.3:c.2158+236A>G
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XP_011520684.1:n.2158+236A>G
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XM_017022944.1:c.2158+236A>G
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XP_016878433.1:n.2158+236A>G
|
|
NM_004380.3:c.2158+236A>G
MANE Select
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NP_004371.2:n.2158+236A>G
|
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