ENST00000553106.6:c.986T>C
MANE Select
|
ENSP00000448059.1:p.Val329Ala
|
|
ENST00000307000.7:c.971T>C
|
ENSP00000303500.2:p.Val324Ala
|
|
ENST00000549247.6:n.745T>C
|
|
|
ENST00000551114.2:n.648T>C
|
|
|
ENST00000553106.5:c.986T>C
|
ENSP00000448059.1:p.Val329Ala
|
|
ENST00000635477.1:c.90T>C
|
|
|
ENST00000635528.1:n.501T>C
|
|
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NM_000277.1:c.986T>C
|
NP_000268.1:p.Val329Ala
|
|
XM_011538422.1:c.929T>C
|
XP_011536724.1:p.Val310Ala
|
|
NM_000277.2:c.986T>C
|
NP_000268.1:p.Val329Ala
|
|
NM_001354304.1:c.986T>C
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NP_001341233.1:p.Val329Ala
|
|
NM_000277.3:c.986T>C
MANE Select
|
NP_000268.1:p.Val329Ala
|
|
NM_001354304.2:c.986T>C
|
NP_001341233.1:p.Val329Ala
|
|