ENST00000691183.1:c.27G>T
|
ENSP00000509954.1:p.Gln9His
|
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ENST00000378842.8:c.27G>T
MANE Select
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ENSP00000368119.4:p.Gln9His
|
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ENST00000378842.7:c.27G>T
|
ENSP00000368119.3:p.Gln9His
|
|
ENST00000450095.6:c.-176G>T
|
ENSP00000401956.2:n.-176G>T
|
|
ENST00000465543.6:n.64G>T
|
|
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ENST00000468099.2:n.99G>T
|
|
|
ENST00000472111.5:n.68G>T
|
|
|
ENST00000473506.6:c.27G>T
|
ENSP00000432839.2:p.Gln9His
|
|
ENST00000473529.5:n.74G>T
|
|
|
ENST00000487381.5:n.53G>T
|
|
|
ENST00000489643.6:n.57G>T
|
|
|
ENST00000554085.5:c.27G>T
|
ENSP00000450419.1:p.Gln9His
|
|
ENST00000554139.5:n.80G>T
|
|
|
ENST00000554550.5:c.27G>T
|
ENSP00000451435.1:p.Gln9His
|
|
ENST00000554638.5:n.51G>T
|
|
|
ENST00000554897.5:c.27G>T
|
ENSP00000450942.1:p.Gln9His
|
|
ENST00000554944.5:n.57G>T
|
|
|
ENST00000555020.5:n.57G>T
|
|
|
ENST00000555214.5:n.36G>T
|
|
|
ENST00000556278.1:c.27G>T
|
ENSP00000451792.1:p.Gln9His
|
|
ENST00000557541.5:n.87G>T
|
|
|
ENST00000605275.1:n.263G>T
|
|
|
NM_000155.3:c.27G>T
|
NP_000146.2:p.Gln9His
|
|
NM_001258332.1:c.-176G>T
|
NP_001245261.1:n.-176G>T
|
|
NM_000155.4:c.27G>T
MANE Select
|
NP_000146.2:p.Gln9His
|
|
NM_001258332.2:c.-176G>T
|
NP_001245261.1:n.-176G>T
|
|