ENST00000368985.8:c.915T>G
MANE Select
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ENSP00000357981.3:p.Gly305=
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ENST00000448301.7:c.687T>G
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ENSP00000408414.2:p.Gly229=
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ENST00000472977.7:c.915T>G
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ENSP00000475176.2:p.Gly305=
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|
ENST00000483930.2:c.*109T>G
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ENSP00000475812.2:n.*109T>G
|
|
ENST00000607427.2:c.915T>G
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ENSP00000475557.2:p.Gly305=
|
|
ENST00000679512.1:c.812T>G
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ENSP00000505113.1:p.Val271Gly
|
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ENST00000679898.1:c.642T>G
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ENSP00000505326.1:p.Gly214=
|
|
ENST00000680288.1:c.765T>G
|
ENSP00000506001.1:p.Gly255=
|
|
ENST00000680311.1:c.646T>G
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ENSP00000505020.1:p.Ter216Gly
|
|
ENST00000680471.1:c.*86T>G
|
ENSP00000506603.1:n.*86T>G
|
|
ENST00000680664.1:c.738T>G
|
ENSP00000506248.1:p.Gly246=
|
|
ENST00000680931.1:c.*265T>G
|
ENSP00000504934.1:n.*265T>G
|
|
ENST00000681357.1:n.305T>G
|
|
|
ENST00000681444.1:c.915T>G
|
ENSP00000505359.1:p.Gly305=
|
|
ENST00000368985.7:c.915T>G
|
ENSP00000357981.3:p.Gly305=
|
|
ENST00000448301.6:c.765T>G
|
ENSP00000408414.1:p.Gly255=
|
|
ENST00000472977.6:c.208T>G
|
|
|
ENST00000483930.1:c.463T>G
|
ENSP00000475812.1:n.463T>G
|
|
NM_001199739.1:c.765T>G
|
NP_001186668.1:p.Gly255=
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|
NM_004079.4:c.915T>G
|
NP_004070.3:p.Gly305=
|
|
NM_004079.5:c.915T>G
MANE Select
|
NP_004070.3:p.Gly305=
|
|
NM_001199739.2:c.765T>G
|
NP_001186668.1:p.Gly255=
|
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