ENST00000368985.8:c.938C>G
MANE Select
|
ENSP00000357981.3:p.Ala313Gly
|
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ENST00000448301.7:c.710C>G
|
ENSP00000408414.2:p.Ala237Gly
|
|
ENST00000472977.7:c.938C>G
|
ENSP00000475176.2:p.Ala313Gly
|
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ENST00000483930.2:c.*132C>G
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ENSP00000475812.2:n.*132C>G
|
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ENST00000607427.2:c.938C>G
|
ENSP00000475557.2:p.Ala313Gly
|
|
ENST00000679512.1:c.835C>G
|
ENSP00000505113.1:p.Gln279Glu
|
|
ENST00000679898.1:c.665C>G
|
ENSP00000505326.1:p.Ala222Gly
|
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ENST00000680288.1:c.788C>G
|
ENSP00000506001.1:p.Ala263Gly
|
|
ENST00000680311.1:c.*21C>G
|
ENSP00000505020.1:n.*21C>G
|
|
ENST00000680471.1:c.*109C>G
|
ENSP00000506603.1:n.*109C>G
|
|
ENST00000680664.1:c.761C>G
|
ENSP00000506248.1:p.Ala254Gly
|
|
ENST00000680931.1:c.*288C>G
|
ENSP00000504934.1:n.*288C>G
|
|
ENST00000681357.1:n.328C>G
|
|
|
ENST00000681444.1:c.938C>G
|
ENSP00000505359.1:p.Ala313Gly
|
|
ENST00000368985.7:c.938C>G
|
ENSP00000357981.3:p.Ala313Gly
|
|
ENST00000448301.6:c.788C>G
|
ENSP00000408414.1:p.Ala263Gly
|
|
ENST00000472977.6:c.231C>G
|
|
|
ENST00000483930.1:c.486C>G
|
ENSP00000475812.1:n.486C>G
|
|
NM_001199739.1:c.788C>G
|
NP_001186668.1:p.Ala263Gly
|
|
NM_004079.4:c.938C>G
|
NP_004070.3:p.Ala313Gly
|
|
NM_004079.5:c.938C>G
MANE Select
|
NP_004070.3:p.Ala313Gly
|
|
NM_001199739.2:c.788C>G
|
NP_001186668.1:p.Ala263Gly
|
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