ENST00000307179.9:c.2234+112A>G
MANE Select
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ENSP00000302239.4:n.2234+112A>G
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|
ENST00000307179.8:c.2234+112A>G
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ENSP00000302239.4:n.2234+112A>G
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|
ENST00000396444.7:c.2234+112A>G
|
ENSP00000379721.3:n.2234+112A>G
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|
ENST00000425032.7:c.1916+112A>G
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ENSP00000412682.3:n.1916+112A>G
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NM_001128610.2:c.2234+112A>G
|
NP_001122082.1:n.2234+112A>G
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|
NM_001283049.1:c.1916+112A>G
|
NP_001269978.1:n.1916+112A>G
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|
NM_005154.4:c.2234+112A>G
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NP_005145.3:n.2234+112A>G
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|
XM_006720761.2:c.2234+112A>G
|
XP_006720824.1:n.2234+112A>G
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|
XM_006720762.2:c.2147+112A>G
|
XP_006720825.1:n.2147+112A>G
|
|
XM_011522193.1:c.2234+112A>G
|
XP_011520495.1:n.2234+112A>G
|
|
XM_011522194.1:c.1562+112A>G
|
XP_011520496.1:n.1562+112A>G
|
|
XM_006720761.3:c.2234+112A>G
|
XP_006720824.1:n.2234+112A>G
|
|
XM_006720762.3:c.2147+112A>G
|
XP_006720825.1:n.2147+112A>G
|
|
XM_011522193.3:c.2234+112A>G
|
XP_011520495.1:n.2234+112A>G
|
|
XM_017022718.1:c.2147+112A>G
|
XP_016878207.1:n.2147+112A>G
|
|
XM_017022719.2:c.2147+112A>G
|
XP_016878208.1:n.2147+112A>G
|
|
XM_017022720.2:c.2147+112A>G
|
XP_016878209.1:n.2147+112A>G
|
|
XM_017022721.2:c.1664+112A>G
|
XP_016878210.1:n.1664+112A>G
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|
XM_017022722.1:c.1664+112A>G
|
XP_016878211.1:n.1664+112A>G
|
|
XM_024450098.1:c.1664+112A>G
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XP_024305866.1:n.1664+112A>G
|
|
NM_005154.5:c.2234+112A>G
MANE Select
|
NP_005145.3:n.2234+112A>G
|
|
NM_001128610.3:c.2234+112A>G
|
NP_001122082.1:n.2234+112A>G
|
|
NM_001283049.2:c.1916+112A>G
|
NP_001269978.1:n.1916+112A>G
|
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