ENST00000355832.10:c.1541G>C
MANE Select
|
ENSP00000348089.5:p.Gly514Ala
|
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ENST00000681632.1:n.1619G>C
|
|
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ENST00000681659.1:c.1526+5202G>C
|
ENSP00000505631.1:n.1526+5202G>C
|
|
ENST00000355832.9:c.1541G>C
|
ENSP00000348089.5:p.Gly514Ala
|
|
ENST00000475116.1:n.131G>C
|
|
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ENST00000623073.3:c.-59G>C
|
ENSP00000485650.1:n.-59G>C
|
|
ENST00000623115.3:c.-214G>C
|
ENSP00000485321.1:n.-214G>C
|
|
ENST00000623318.1:c.-59G>C
|
ENSP00000485423.1:n.-59G>C
|
|
ENST00000623788.1:n.540G>C
|
|
|
NM_000124.3:c.1541G>C
|
NP_000115.1:p.Gly514Ala
|
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NM_001346440.1:c.1541G>C
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NP_001333369.1:p.Gly514Ala
|
|
NM_000124.4:c.1541G>C
MANE Select
|
NP_000115.1:p.Gly514Ala
|
|
NM_001346440.2:c.1541G>C
|
NP_001333369.1:p.Gly514Ala
|
|