ENST00000261208.8:c.1311G>A
MANE Select
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ENSP00000261208.3:p.Glu437=
|
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ENST00000261208.7:c.1311G>A
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ENSP00000261208.3:p.Glu437=
|
|
ENST00000538703.5:c.1311G>A
|
ENSP00000440861.1:p.Glu437=
|
|
ENST00000541929.5:c.687G>A
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ENSP00000446364.1:p.Glu229=
|
|
ENST00000544080.6:c.*740G>A
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ENSP00000439385.2:n.*740G>A
|
|
ENST00000546999.5:c.*740G>A
|
ENSP00000447675.1:n.*740G>A
|
|
NM_001258333.1:c.687G>A
|
NP_001245262.1:p.Glu229=
|
|
NM_001258334.1:c.1311G>A
|
NP_001245263.1:p.Glu437=
|
|
NM_002108.3:c.1311G>A
|
NP_002099.1:p.Glu437=
|
|
XM_011538249.1:c.459G>A
|
XP_011536551.1:p.Glu153=
|
|
XM_011538249.2:c.459G>A
|
XP_011536551.1:p.Glu153=
|
|
XM_017019246.1:c.381G>A
|
XP_016874735.1:p.Glu127=
|
|
NM_002108.4:c.1311G>A
MANE Select
|
NP_002099.1:p.Glu437=
|
|
NM_001258334.2:c.1311G>A
|
NP_001245263.1:p.Glu437=
|
|
NM_001258333.2:c.687G>A
|
NP_001245262.1:p.Glu229=
|
|