ENST00000324856.13:c.-2T>G
MANE Select
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ENSP00000320485.7:n.-2T>G
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ENST00000430799.7:c.-13+2785T>G
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ENSP00000390317.3:n.-13+2785T>G
|
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ENST00000637465.1:c.-13+302T>G
|
ENSP00000490650.1:n.-13+302T>G
|
|
ENST00000324856.11:c.-2T>G
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ENSP00000320485.7:n.-2T>G
|
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NM_006015.4:c.-2T>G , LRG_875t1:c.-2T>G
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NP_006006.3:n.-2T>G
|
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NM_139135.2:c.-2T>G
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NP_624361.1:n.-2T>G
|
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XM_011542542.1:c.4A>C
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XP_011540844.1:p.Ile2Leu
|
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NM_006015.5:c.-2T>G
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NP_006006.3:n.-2T>G
|
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NM_139135.3:c.-2T>G
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NP_624361.1:n.-2T>G
|
|
NM_006015.6:c.-2T>G
MANE Select
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NP_006006.3:n.-2T>G
|
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NM_139135.4:c.-2T>G
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NP_624361.1:n.-2T>G
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