ENST00000481739.2:c.383C>G
MANE Select
|
ENSP00000419692.1:p.Ala128Gly
|
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ENST00000672570.1:c.302C>G
|
ENSP00000500402.1:p.Ala101Gly
|
|
ENST00000356384.4:n.793C>G
|
|
|
ENST00000481739.1:c.383C>G
|
ENSP00000419692.1:p.Ala128Gly
|
|
NM_001291920.1:c.302C>G
|
NP_001278849.1:p.Ala101Gly
|
|
NM_001291921.1:c.92C>G
|
NP_001278850.1:p.Ala31Gly
|
|
NM_002957.5:c.383C>G
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NP_002948.1:p.Ala128Gly
|
|
NM_002957.6:c.383C>G
MANE Select
|
NP_002948.1:p.Ala128Gly
|
|
NM_001291921.2:c.92C>G
|
NP_001278850.1:p.Ala31Gly
|
|
NM_001291920.2:c.302C>G
|
NP_001278849.1:p.Ala101Gly
|
|