ENST00000368985.8:c.962G>C
MANE Select
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ENSP00000357981.3:p.Gly321Ala
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ENST00000448301.7:c.734G>C
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ENSP00000408414.2:p.Gly245Ala
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ENST00000472977.7:c.962G>C
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ENSP00000475176.2:p.Gly321Ala
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ENST00000483930.2:c.*156G>C
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ENSP00000475812.2:n.*156G>C
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ENST00000607427.2:c.962G>C
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ENSP00000475557.2:p.Gly321Ala
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ENST00000679512.1:c.859G>C
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ENSP00000505113.1:p.Gly287Arg
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ENST00000679898.1:c.689G>C
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ENSP00000505326.1:p.Gly230Ala
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ENST00000680288.1:c.812G>C
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ENSP00000506001.1:p.Gly271Ala
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ENST00000680311.1:c.*45G>C
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ENSP00000505020.1:n.*45G>C
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ENST00000680471.1:c.*133G>C
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ENSP00000506603.1:n.*133G>C
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ENST00000680664.1:c.785G>C
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ENSP00000506248.1:p.Gly262Ala
|
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ENST00000680931.1:c.*312G>C
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ENSP00000504934.1:n.*312G>C
|
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ENST00000681357.1:n.352G>C
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|
|
ENST00000681444.1:c.962G>C
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ENSP00000505359.1:p.Gly321Ala
|
|
ENST00000368985.7:c.962G>C
|
ENSP00000357981.3:p.Gly321Ala
|
|
ENST00000448301.6:c.812G>C
|
ENSP00000408414.1:p.Gly271Ala
|
|
ENST00000472977.6:c.255G>C
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|
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ENST00000483930.1:c.510G>C
|
ENSP00000475812.1:n.510G>C
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NM_001199739.1:c.812G>C
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NP_001186668.1:p.Gly271Ala
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NM_004079.4:c.962G>C
|
NP_004070.3:p.Gly321Ala
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NM_004079.5:c.962G>C
MANE Select
|
NP_004070.3:p.Gly321Ala
|
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NM_001199739.2:c.812G>C
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NP_001186668.1:p.Gly271Ala
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