ENST00000428216.4:c.189G>T
MANE Select
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ENSP00000401980.2:p.Gln63His
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ENST00000416600.6:c.-132+2965G>T
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ENSP00000413749.2:n.-132+2965G>T
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ENST00000428216.3:c.189G>T
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ENSP00000401980.2:p.Gln63His
|
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NM_001206491.1:c.-132+2965G>T
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NP_001193420.1:n.-132+2965G>T
|
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NM_020746.4:c.189G>T
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NP_065797.2:p.Gln63His
|
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NR_037921.1:n.361G>T
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NM_020746.5:c.189G>T
MANE Select
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NP_065797.2:p.Gln63His
|
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NR_037921.2:n.326G>T
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|
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NM_001206491.2:c.-132+2965G>T
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NP_001193420.1:n.-132+2965G>T
|
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NM_001385663.1:c.-359G>T
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NP_001372592.1:n.-359G>T
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