ENST00000265512.12:c.878G>C
MANE Select
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ENSP00000265512.7:p.Gly293Ala
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ENST00000265512.11:c.878G>C
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ENSP00000265512.7:p.Gly293Ala
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ENST00000505590.5:c.935G>C
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ENSP00000425416.1:p.Gly312Ala
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ENST00000506705.5:c.*852G>C
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ENSP00000426667.1:n.*852G>C
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ENST00000508393.5:c.935G>C
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ENSP00000424630.1:p.Gly312Ala
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ENST00000509471.5:c.334-578G>C
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ENSP00000424583.1:n.334-578G>C
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ENST00000629236.2:c.878G>C
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ENSP00000486450.1:p.Gly293Ala
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NM_000670.3:c.878G>C
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NP_000661.2:p.Gly293Ala
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NM_000670.4:c.878G>C
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NP_000661.2:p.Gly293Ala
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NM_001306171.1:c.935G>C
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NP_001293100.1:p.Gly312Ala
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NM_001306172.1:c.935G>C
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NP_001293101.1:p.Gly312Ala
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NR_037884.1:n.429-6245C>G
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XR_938685.1:n.1106G>C
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XR_938686.1:n.1097G>C
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XR_938687.1:n.970G>C
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NM_000670.5:c.878G>C
MANE Select
|
NP_000661.2:p.Gly293Ala
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NM_001306171.2:c.935G>C
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NP_001293100.1:p.Gly312Ala
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NM_001306172.2:c.935G>C
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NP_001293101.1:p.Gly312Ala
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