ENST00000398603.6:c.337-281C=
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ENSP00000381604.1:n.337-281C=
|
|
ENST00000398606.10:c.341C=
MANE Select
|
ENSP00000381607.3:p.Ala114=
|
|
ENST00000646888.1:c.*57C=
|
ENSP00000494477.1:n.*57C=
|
|
ENST00000398603.5:c.337-281C=
|
ENSP00000381604.1:n.337-281C=
|
|
ENST00000398606.7:c.341C=
|
ENSP00000381607.3:p.Ala114=
|
|
ENST00000467591.1:n.452C=
|
|
|
ENST00000494593.1:n.1136C=
|
|
|
ENST00000495996.1:c.5C=
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ENSP00000484686.1:p.Ala2=
|
|
ENST00000498765.5:c.404C=
|
|
|
NM_000852.3:c.341C= , LRG_723t1:c.341C=
|
NP_000843.1:p.Ala114=
|
|
NM_000852.4:c.341C=
MANE Select
|
NP_000843.1:p.Ala114=
|
|