ENST00000527168.6:n.689A>C
|
|
|
ENST00000529110.2:c.674A>C
|
ENSP00000435349.2:p.Asp225Ala
|
|
ENST00000529957.6:n.648A>C
|
|
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ENST00000683366.1:c.*322A>C
|
ENSP00000507283.1:n.*322A>C
|
|
ENST00000683887.1:c.638A>C
|
ENSP00000506886.1:p.Asp213Ala
|
|
ENST00000684100.1:n.584A>C
|
|
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ENST00000684126.1:n.648A>C
|
|
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ENST00000684688.1:n.1215A>C
|
|
|
ENST00000204679.9:c.590A>C
MANE Select
|
ENSP00000204679.4:p.Asp197Ala
|
|
ENST00000204679.8:c.590A>C
|
ENSP00000204679.4:p.Asp197Ala
|
|
ENST00000527076.1:n.1737A>C
|
|
|
ENST00000527168.5:n.757A>C
|
|
|
ENST00000529957.5:n.689A>C
|
|
|
NM_032520.4:c.590A>C
|
NP_115909.1:p.Asp197Ala
|
|
XM_017023782.1:c.638A>C
|
XP_016879271.1:p.Asp213Ala
|
|
XM_017023783.1:c.230A>C
|
XP_016879272.1:p.Asp77Ala
|
|
NM_032520.5:c.590A>C
MANE Select
|
NP_115909.1:p.Asp197Ala
|
|