ENST00000375559.8:c.1006A>G
MANE Select
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ENSP00000364709.3:p.Met336Val
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|
ENST00000375551.7:c.996A>G
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ENSP00000364701.3:p.Ala332=
|
|
ENST00000375559.7:c.1006A>G
|
ENSP00000364709.3:p.Met336Val
|
|
ENST00000409306.5:c.1002A>G
|
ENSP00000387092.1:p.Ala334=
|
|
NM_000504.3:c.1006A>G , LRG_548t1:c.1006A>G
|
NP_000495.1:p.Met336Val
|
|
NM_001312674.1:c.874A>G
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NP_001299603.1:p.Met292Val
|
|
NM_001312675.1:c.996A>G
|
NP_001299604.1:p.Ala332=
|
|
NM_000504.4:c.1006A>G
MANE Select
|
NP_000495.1:p.Met336Val
|
|
NM_001312674.2:c.874A>G
|
NP_001299603.1:p.Met292Val
|
|
NM_001312675.2:c.996A>G
|
NP_001299604.1:p.Ala332=
|
|