ENST00000261208.8:c.755G>A
MANE Select
|
ENSP00000261208.3:p.Gly252Asp
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ENST00000261208.7:c.755G>A
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ENSP00000261208.3:p.Gly252Asp
|
|
ENST00000538703.5:c.755G>A
|
ENSP00000440861.1:p.Gly252Asp
|
|
ENST00000541929.5:c.131G>A
|
ENSP00000446364.1:p.Gly44Asp
|
|
ENST00000544080.6:c.*184G>A
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ENSP00000439385.2:n.*184G>A
|
|
ENST00000546999.5:c.*184G>A
|
ENSP00000447675.1:n.*184G>A
|
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ENST00000549376.1:n.148G>A
|
|
|
ENST00000551562.1:n.15G>A
|
|
|
ENST00000552509.5:c.719G>A
|
ENSP00000450372.1:p.Gly240Asp
|
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NM_001258333.1:c.131G>A
|
NP_001245262.1:p.Gly44Asp
|
|
NM_001258334.1:c.755G>A
|
NP_001245263.1:p.Gly252Asp
|
|
NM_002108.3:c.755G>A
|
NP_002099.1:p.Gly252Asp
|
|
XM_011538249.1:c.3+2187G>A
|
XP_011536551.1:n.3+2187G>A
|
|
XM_011538249.2:c.3+2187G>A
|
XP_011536551.1:n.3+2187G>A
|
|
NM_002108.4:c.755G>A
MANE Select
|
NP_002099.1:p.Gly252Asp
|
|
NM_001258334.2:c.755G>A
|
NP_001245263.1:p.Gly252Asp
|
|
NM_001258333.2:c.131G>A
|
NP_001245262.1:p.Gly44Asp
|
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