ENST00000355773.6:c.978+17A>G
MANE Select
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ENSP00000348019.5:n.978+17A>G
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ENST00000355773.5:c.978+17A>G
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ENSP00000348019.5:n.978+17A>G
|
|
NM_012434.4:c.978+17A>G
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NP_036566.1:n.978+17A>G
|
|
XM_005248710.2:c.927+17A>G
|
XP_005248767.1:n.927+17A>G
|
|
XM_005248711.1:c.780+17A>G
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XP_005248768.1:n.780+17A>G
|
|
XM_011535750.1:c.978+17A>G
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XP_011534052.1:n.978+17A>G
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|
NM_012434.5:c.978+17A>G
MANE Select
|
NP_036566.1:n.978+17A>G
|
|
NM_001382629.1:c.747+17A>G
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NP_001369558.1:n.747+17A>G
|
|
NM_001382630.1:c.978+17A>G
|
NP_001369559.1:n.978+17A>G
|
|
NM_001382631.1:c.999+17A>G
|
NP_001369560.1:n.999+17A>G
|
|
NM_001382632.1:c.891+17A>G
|
NP_001369561.1:n.891+17A>G
|
|
NM_001382633.1:c.978+17A>G
|
NP_001369562.1:n.978+17A>G
|
|
NM_001382634.1:c.820-6340A>G
|
NP_001369563.1:n.820-6340A>G
|
|
NM_001382635.1:c.975+17A>G
|
NP_001369564.1:n.975+17A>G
|
|
NM_001382636.1:c.660+17A>G
|
NP_001369565.1:n.660+17A>G
|
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