ENST00000634878.2:c.741+51A>G
|
|
|
ENST00000642944.1:c.1054+51A>G
|
ENSP00000495674.1:n.1054+51A>G
|
|
ENST00000643023.1:c.1291+51A>G
|
ENSP00000495664.1:n.1291+51A>G
|
|
ENST00000643584.1:c.1228+51A>G
|
ENSP00000494987.1:n.1228+51A>G
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|
ENST00000646804.1:c.1054+51A>G
|
ENSP00000493977.1:n.1054+51A>G
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|
ENST00000646932.1:c.1228+51A>G
MANE Select
|
ENSP00000494360.1:n.1228+51A>G
|
|
ENST00000647361.1:c.*1021+51A>G
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ENSP00000494607.1:n.*1021+51A>G
|
|
ENST00000378654.8:c.1228+51A>G
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ENSP00000367923.3:n.1228+51A>G
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|
ENST00000467222.1:n.536+51A>G
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|
|
ENST00000493152.6:c.79+51A>G
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ENSP00000489055.1:n.79+51A>G
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|
ENST00000634878.1:c.741+51A>G
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|
|
NM_003850.2:c.1228+51A>G
|
NP_003841.1:n.1228+51A>G
|
|
XM_011535292.1:c.991+51A>G
|
XP_011533594.1:n.991+51A>G
|
|
XM_011535293.1:c.826+51A>G
|
XP_011533595.1:n.826+51A>G
|
|
NM_003850.3:c.1228+51A>G
MANE Select
|
NP_003841.1:n.1228+51A>G
|
|