ENST00000555238.6:c.1779T>A
MANE Select
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ENSP00000451300.1:p.Asp593Glu
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ENST00000355058.7:c.1779T>A
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ENSP00000347169.3:p.Asp593Glu
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ENST00000356296.8:c.1635T>A
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ENSP00000348644.4:p.Asp545Glu
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ENST00000359560.7:c.1746T>A
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ENSP00000352563.3:p.Asp582Glu
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ENST00000535282.5:c.1635T>A
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ENSP00000441258.2:p.Asp545Glu
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ENST00000544991.7:c.1194T>A
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ENSP00000446001.3:p.Asp398Glu
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ENST00000554521.6:c.1161T>A
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ENSP00000450817.2:p.Asp387Glu
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ENST00000554546.5:c.1602T>A
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ENSP00000452416.1:p.Asp534Glu
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ENST00000555238.5:c.1779T>A
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ENSP00000451300.1:p.Asp593Glu
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|
ENST00000555394.5:c.1635T>A
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ENSP00000451625.1:p.Asp545Glu
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|
ENST00000555738.6:c.1308T>A
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ENSP00000452069.2:p.Asp436Glu
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ENST00000556772.5:c.1347T>A
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ENSP00000451513.1:p.Asp449Glu
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ENST00000557597.5:c.1746T>A
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ENSP00000451117.1:p.Asp582Glu
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|
ENST00000559312.5:c.1194T>A
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ENSP00000452888.1:p.Asp398Glu
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|
ENST00000560335.5:c.1341T>A
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ENSP00000453209.1:p.Asp447Glu
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NM_001005743.1:c.1779T>A
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NP_001005743.1:p.Asp593Glu
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NM_001005744.1:c.1635T>A
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NP_001005744.1:p.Asp545Glu
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NM_001005745.1:c.1602T>A
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NP_001005745.1:p.Asp534Glu
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NM_003744.5:c.1746T>A
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NP_003735.3:p.Asp582Glu
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|
XM_005268142.3:c.1779T>A
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XP_005268199.1:p.Asp593Glu
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XM_005268144.3:c.1746T>A
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XP_005268201.1:p.Asp582Glu
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|
XM_005268145.3:c.1737T>A
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XP_005268202.1:p.Asp579Glu
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|
XM_005268146.3:c.1635T>A
|
XP_005268203.1:p.Asp545Glu
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|
XM_011537253.1:c.1779T>A
|
XP_011535555.1:p.Asp593Glu
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|
XM_011537254.1:c.1779T>A
|
XP_011535556.1:p.Asp593Glu
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|
XM_011537255.1:c.1779T>A
|
XP_011535557.1:p.Asp593Glu
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|
XM_011537256.1:c.1770T>A
|
XP_011535558.1:p.Asp590Glu
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|
XM_011537257.1:c.1746T>A
|
XP_011535559.1:p.Asp582Glu
|
|
XM_011537258.1:c.1746T>A
|
XP_011535560.1:p.Asp582Glu
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|
XM_011537259.1:c.1737T>A
|
XP_011535561.1:p.Asp579Glu
|
|
XM_011537260.1:c.1635T>A
|
XP_011535562.1:p.Asp545Glu
|
|
XM_011537261.1:c.1626T>A
|
XP_011535563.1:p.Asp542Glu
|
|
XM_011537262.1:c.1485T>A
|
XP_011535564.1:p.Asp495Glu
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|
XM_011537263.1:c.1341T>A
|
XP_011535565.1:p.Asp447Glu
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|
XM_011537264.1:c.1308T>A
|
XP_011535566.1:p.Asp436Glu
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|
NM_001320114.1:c.1635T>A
|
NP_001307043.1:p.Asp545Glu
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|
NM_001005743.2:c.1779T>A
MANE Select
|
NP_001005743.1:p.Asp593Glu
|
|
NM_001005744.2:c.1635T>A
|
NP_001005744.1:p.Asp545Glu
|
|
NM_001005745.2:c.1602T>A
|
NP_001005745.1:p.Asp534Glu
|
|
NM_001320114.2:c.1635T>A
|
NP_001307043.1:p.Asp545Glu
|
|
NM_003744.6:c.1746T>A
|
NP_003735.3:p.Asp582Glu
|
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