ENST00000309755.9:c.1452G>T
MANE Select
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ENSP00000312397.4:p.Gly484=
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ENST00000309755.8:c.1452G>T
|
ENSP00000312397.4:p.Gly484=
|
|
ENST00000447439.6:n.1508G>T
|
|
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ENST00000504208.5:c.*336G>T
|
ENSP00000423585.1:n.*336G>T
|
|
ENST00000506491.5:c.1206G>T
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ENSP00000424828.1:p.Gly402=
|
|
ENST00000506873.5:n.975G>T
|
|
|
ENST00000508657.5:c.1356G>T
|
ENSP00000422099.1:p.Gly452=
|
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ENST00000509694.1:n.245G>T
|
|
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NM_001257194.1:c.1356G>T
|
NP_001244123.1:p.Gly452=
|
|
NM_001257195.1:c.1206G>T
|
NP_001244124.1:p.Gly402=
|
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NM_017415.2:c.1452G>T
|
NP_059111.2:p.Gly484=
|
|
NM_017415.3:c.1452G>T
MANE Select
|
NP_059111.2:p.Gly484=
|
|
NM_001257195.2:c.1206G>T
|
NP_001244124.1:p.Gly402=
|
|