ENST00000383032.6:c.-266+7923A>G
MANE Select
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ENSP00000372499.1:n.-266+7923A>G
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|
ENST00000346432.3:c.-171+7923A>G
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ENSP00000328879.4:n.-171+7923A>G
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|
ENST00000355162.6:c.-235+7923A>G
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ENSP00000347289.2:n.-235+7923A>G
|
|
ENST00000383032.5:c.-266+7923A>G
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ENSP00000372499.1:n.-266+7923A>G
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|
NM_033284.1:c.-266+7923A>G
|
NP_150600.1:n.-266+7923A>G
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|
NM_134258.1:c.-235+7923A>G
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NP_599020.1:n.-235+7923A>G
|
|
NM_134259.1:c.-171+7923A>G
|
NP_599021.1:n.-171+7923A>G
|
|
XM_017030086.1:c.-266+7923A>G
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XP_016885575.1:n.-266+7923A>G
|
|
XM_017030087.1:c.-266+7923A>G
|
XP_016885576.1:n.-266+7923A>G
|
|
XM_024452497.1:c.-266+7923A>G
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XP_024308265.1:n.-266+7923A>G
|
|
NM_033284.2:c.-266+7923A>G
MANE Select
|
NP_150600.1:n.-266+7923A>G
|
|
NM_134258.2:c.-235+7923A>G
|
NP_599020.1:n.-235+7923A>G
|
|
NM_134259.2:c.-171+7923A>G
|
NP_599021.1:n.-171+7923A>G
|
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