ENST00000261208.8:c.1307G>A
MANE Select
|
ENSP00000261208.3:p.Gly436Glu
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ENST00000261208.7:c.1307G>A
|
ENSP00000261208.3:p.Gly436Glu
|
|
ENST00000538703.5:c.1307G>A
|
ENSP00000440861.1:p.Gly436Glu
|
|
ENST00000541929.5:c.683G>A
|
ENSP00000446364.1:p.Gly228Glu
|
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ENST00000544080.6:c.*736G>A
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ENSP00000439385.2:n.*736G>A
|
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ENST00000546999.5:c.*736G>A
|
ENSP00000447675.1:n.*736G>A
|
|
NM_001258333.1:c.683G>A
|
NP_001245262.1:p.Gly228Glu
|
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NM_001258334.1:c.1307G>A
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NP_001245263.1:p.Gly436Glu
|
|
NM_002108.3:c.1307G>A
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NP_002099.1:p.Gly436Glu
|
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XM_011538249.1:c.455G>A
|
XP_011536551.1:p.Gly152Glu
|
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XM_011538249.2:c.455G>A
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XP_011536551.1:p.Gly152Glu
|
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XM_017019246.1:c.377G>A
|
XP_016874735.1:p.Gly126Glu
|
|
NM_002108.4:c.1307G>A
MANE Select
|
NP_002099.1:p.Gly436Glu
|
|
NM_001258334.2:c.1307G>A
|
NP_001245263.1:p.Gly436Glu
|
|
NM_001258333.2:c.683G>A
|
NP_001245262.1:p.Gly228Glu
|
|