ENST00000553106.6:c.1154T>A
MANE Select
|
ENSP00000448059.1:p.Leu385His
|
|
ENST00000307000.7:c.1139T>A
|
ENSP00000303500.2:p.Leu380His
|
|
ENST00000549247.6:n.913T>A
|
|
|
ENST00000551114.2:n.816T>A
|
|
|
ENST00000553106.5:c.1154T>A
|
ENSP00000448059.1:p.Leu385His
|
|
ENST00000635477.1:c.258T>A
|
|
|
ENST00000635528.1:n.669T>A
|
|
|
NM_000277.1:c.1154T>A
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NP_000268.1:p.Leu385Gln
|
|
XM_011538422.1:c.1097T>A
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XP_011536724.1:p.Leu366His
|
|
NM_000277.2:c.1154T>A
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NP_000268.1:p.Leu385His
|
|
NM_001354304.1:c.1154T>A
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NP_001341233.1:p.Leu385His
|
|
NM_000277.3:c.1154T>A
MANE Select
|
NP_000268.1:p.Leu385His
|
|
NM_001354304.2:c.1154T>A
|
NP_001341233.1:p.Leu385His
|
|