ENST00000529510.6:n.989G>T
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ENST00000697845.1:n.913G>T
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ENST00000697846.1:n.989G>T
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ENST00000697847.1:n.989G>T
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ENST00000697848.1:n.989G>T
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|
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ENST00000697849.1:n.2028G>T
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ENST00000697850.1:n.989G>T
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ENST00000697851.1:n.2349G>T
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ENST00000638186.1:n.1063G>T
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ENST00000638360.1:n.895G>T
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ENST00000638925.1:n.996G>T
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ENST00000650539.1:n.1165G>T
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ENST00000330775.9:c.759G>T
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ENSP00000476242.2:p.Gln253His
|
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ENST00000357590.9:c.759G>T
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ENSP00000476176.2:p.Gln253His
|
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ENST00000524428.5:n.1081G>T
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ENST00000525039.5:n.1183G>T
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ENST00000525102.5:n.1517G>T
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ENST00000525372.5:n.760G>T
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|
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ENST00000526275.5:n.1541G>T
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|
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ENST00000526626.6:n.722G>T
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|
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ENST00000527992.5:n.987G>T
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|
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ENST00000529510.5:n.533G>T
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|
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ENST00000530407.5:n.909G>T
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|
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ENST00000532085.1:n.3370G>T
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|
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ENST00000532888.6:n.1055G>T
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|
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ENST00000538950.5:c.540G>T
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ENSP00000475991.2:p.Gln180His
|
|
ENST00000545985.5:c.759G>T
|
ENSP00000475241.2:p.Gln253His
|
|
NM_001164277.1:c.759G>T , LRG_187t1:c.759G>T
|
NP_001157749.1:p.Gln253His
|
|
NM_001164278.1:c.759G>T
|
NP_001157750.1:p.Gln253His
|
|
NM_001164279.1:c.540G>T
|
NP_001157751.1:p.Gln180His
|
|
NM_001164280.1:c.759G>T
|
NP_001157752.1:p.Gln253His
|
|
NM_001467.5:c.759G>T
|
NP_001458.1:p.Gln253His
|
|
NM_001164278.2:c.759G>T
|
NP_001157750.1:p.Gln253His
|
|
NM_001164279.2:c.540G>T
|
NP_001157751.1:p.Gln180His
|
|
NM_001164280.2:c.759G>T
|
NP_001157752.1:p.Gln253His
|
|
NM_001467.6:c.759G>T
|
NP_001458.1:p.Gln253His
|
|
NM_001164277.2:c.759G>T
MANE Select
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NP_001157749.1:p.Gln253His
|
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